Variants
Sign InSign Up

rs747614356

  • Likely benign

Your Genotype

Sign In

Description

Reference Allele

A


Alternative Allele

G

T

Chromosome

16


Location

2088529


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5343A>G (p.Pro1781=)


Allele

G


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.