Variants
Sign InSign Up

rs45517422

  • Uncertain significance

Your Genotype

Sign In

Description

Reference Allele

G


Alternative Allele

C

Chromosome

16


Location

2088562


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5376G>C (p.Gln1792His)


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.