Variants
Sign InSign Up

rs188146738

  • Benign

Your Genotype

Sign In

Description

Reference Allele

C


Alternative Allele

T

Chromosome

19


Location

7610801


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_020902.2(CAMSAP3):c.994+8C>T


Allele

T


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.