Variants
Sign InSign Up

rs188395735

  • Benign

Your Genotype

Sign In

Description

Reference Allele

G


Alternative Allele

A

Chromosome

22


Location

38082672


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_013356.3(SLC16A8):c.202C>T (p.Leu68Phe)


Allele

A


Clinical Significance

Benign

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.