Variants
Sign InSign Up

rs397515370

  • Pathogenic

Your Genotype

Sign In

Description

Reference Allele

T


Alternative Allele

G

Chromosome

22


Location

37974200


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.698-2A>C


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.