Variants
Sign InSign Up

rs1416891382

  • Uncertain significance

Your Genotype

Sign In

Description

Reference Allele

T


Alternative Allele

G

Chromosome

9


Location

110747762


Variant Type

SNP

Genes

ClinVar

Name

NM_005592.4(MUSK):c.875T>G (p.Phe292Cys)


Allele

G


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.