Variants
Sign InSign Up

rs150567570

  • Likely benign

Your Genotype

Sign In

Description

Reference Allele

G


Alternative Allele

A

T

Chromosome

19


Location

7640769


Variant Type

SNP

Genes

ClinVar

Name

NM_006949.4(STXBP2):c.285G>A (p.Pro95=)


Allele

A


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.