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Q: What is the clinical significance of unknown (GSTT1, NT_187633.1:270737 C>T)?
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A: The variant unknown in gene GSTT1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001819: synonymous_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (GSTT1, NT_187633.1:273567 C>T)?
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A: The variant unknown in gene GSTT1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001623: 5_prime_UTR_variant,SO:0001627: intron_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (GSTT1, NT_187633.1:273606 C>T)?
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A: The variant unknown in gene GSTT1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001623: 5_prime_UTR_variant,SO:0001627: intron_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (GSTT1, NT_187633.1:273613 G>A)?
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A: The variant unknown in gene GSTT1 is classified as 'Likely_benign' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001623: 5_prime_UTR_variant,SO:0001627: intron_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (GSTT1, NT_187633.1:275897 C>T)?
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A: The variant unknown in gene GSTT1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001623: 5_prime_UTR_variant,SO:0001627: intron_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL3L1, NT_187661.1:251046 G>A)?
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A: The variant unknown in gene CCL3L1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001619: non-coding_transcript_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL3L1, NT_187661.1:251083 A>G)?
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A: The variant unknown in gene CCL3L1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001619: non-coding_transcript_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL3L1, NT_187661.1:252336 C>T)?
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A: The variant unknown in gene CCL3L1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001619: non-coding_transcript_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL3L1, NT_187661.1:252338 A>G)?
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A: The variant unknown in gene CCL3L1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001619: non-coding_transcript_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL3L1, NT_187661.1:252354 C>T)?
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A: The variant unknown in gene CCL3L1 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant,SO:0001619: non-coding_transcript_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL4L2, NT_187661.1:268116 G>C)?
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A: The variant unknown in gene CCL4L2 is classified as 'Likely_benign' for not_provided. Molecular consequence: SO:0001627: intron_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:C3661900. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL4L2, NT_187661.1:268179 C>G)?
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A: The variant unknown in gene CCL4L2 is classified as 'Likely_benign' for not_provided. Molecular consequence: SO:0001627: intron_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:C3661900. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (CCL4L2, NT_187661.1:268201 G>A)?
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A: The variant unknown in gene CCL4L2 is classified as 'Likely_benign' for not_provided. Molecular consequence: SO:0001583: missense_variant,SO:0001619: non-coding_transcript_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:C3661900. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:273340 T>A)?
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A: The variant unknown in gene LILRA3 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:273622 G>A)?
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A: The variant unknown in gene LILRA3 is classified as 'Likely_benign' for not_provided. Molecular consequence: SO:0001819: synonymous_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:C3661900. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:273632 G>A)?
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A: The variant unknown in gene LILRA3 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:273661 G>A)?
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A: The variant unknown in gene LILRA3 is classified as 'Likely_benign' for not_provided. Molecular consequence: SO:0001819: synonymous_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:C3661900. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:273753 G>A)?
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A: The variant unknown in gene LILRA3 is classified as 'Benign' for not_provided. Molecular consequence: SO:0001583: missense_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:C3661900. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:273806 G>A)?
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A: The variant unknown in gene LILRA3 is classified as 'Likely_benign' for not_specified. Molecular consequence: SO:0001583: missense_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:273866 A>C)?
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A: The variant unknown in gene LILRA3 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:274185 C>T)?
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A: The variant unknown in gene LILRA3 is classified as 'Likely_benign' for not_provided. Molecular consequence: SO:0001627: intron_variant,SO:0001819: synonymous_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:C3661900. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:274366 G>C)?
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A: The variant unknown in gene LILRA3 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (LILRA3, NT_187693.1:275068 T>C)?
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A: The variant unknown in gene LILRA3 is classified as 'Uncertain_significance' for not_specified. Molecular consequence: SO:0001583: missense_variant. Variant type: single_nucleotide_variant. Disease database links: MedGen:CN169374. Review status: criteria provided, single submitter.
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Q: What is the clinical significance of unknown (ABO, NW_009646201.1:83614 TC>T)?
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A: The variant unknown in gene ABO is classified as 'Benign' for not_provided|ABO_blood_group_system. Molecular consequence: SO:0001589: frameshift_variant. Variant type: Deletion. Disease database links: MedGen:C3661900|Human_Phenotype_Ontology:HP:0032224,MedGen:C0000778,OMIM:616093. Review status: criteria provided, single submitter.
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