Variants
Sign InSign Up

rs1601879433

  • Likely benign

Your Genotype

Sign In

Description

Reference Allele

A


Alternative Allele

T

Chromosome

22


Location

37974173


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_006941.4(SOX10):c.723T>A (p.Pro241=)


Allele

T


Clinical Significance

Likely benign

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

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