Variants
Sign InSign Up

rs772865175

  • Benign/Likely benign

Your Genotype

Sign In

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

Reference Allele

C


Alternative Allele

G

T

Chromosome

16


Location

2088298


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5232C>T (p.Leu1744=)


Allele

T


Clinical Significance

Benign/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.