Variants
Sign InSign Up

rs3811005

  • 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

G


Alternative Allele

C

T

Chromosome

1


Location

115704914


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001232.4(CASQ2):c.939+278C>G


Allele

C


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.