Variants
Sign InSign Up

rs1932464492

  • Pathogenic

Your Genotype

Sign In

Description

Reference Allele

A


Alternative Allele

G

Chromosome

22


Location

37983462


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.323T>C (p.Met108Thr)


Allele

G


Clinical Significance

Pathogenic

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.