Variants
Sign InSign Up

rs777365329

  • Uncertain significance

Your Genotype

Sign In

Description

Reference Allele

C


Alternative Allele

T

Chromosome

2


Location

219157536


Variant Type

SNP

Genes

ClinVar

Name

NM_024782.3(NHEJ1):c.326G>A (p.Arg109Gln)


Allele

T


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.