Variants
Sign InSign Up

rs1932463844

  • Likely pathogenic

Your Genotype

Sign In

Description

Reference Allele

A


Alternative Allele

C

Chromosome

22


Location

37983450


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.335T>G (p.Met112Arg)


Allele

C


Clinical Significance

Likely pathogenic

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

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