Variants
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rs8141371

  • Likely benign

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Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

37972563


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.*932G>A


Allele

T


Clinical Significance

Likely benign

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