Variants
Sign InSign Up

rs1060500918

  • Uncertain significance
  • Uncertain significance

Your Genotype

Sign In

Description

Reference Allele

G


Alternative Allele

A

T

Chromosome

16


Location

2088589


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5403G>T (p.Glu1801Asp)


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.