Variants
Sign InSign Up

rs201329593

  • Likely benign

Your Genotype

Sign In

Description

Reference Allele

C


Alternative Allele

T

Chromosome

16


Location

2088350


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_000548.5(TSC2):c.5259+25C>T


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.