Variants
Sign InSign Up

rs375443308

  • Likely benign

Your Genotype

Sign In

Description

Reference Allele

G


Alternative Allele

A

C

T

Chromosome

16


Location

2089804


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001009944.3(PKD1):c.12835C>A (p.Arg4279=)


Allele

T


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.