Variants
Sign InSign Up

rs533778281

  • Uncertain significance

Your Genotype

Sign In

Description

Regulation of SOX10 expression

Reference Allele

G


Alternative Allele

C

Chromosome

22


Location

38016774


Variant Type

SNP

Genes

ClinVar

Name

NM_001301130.2(POLR2F):c.453-24294G>C


Allele

C


Clinical Significance

Uncertain significance

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

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