Variants
Genes
Phenotypes
Pricing
Sign InSign Up

rs7023478

    Your Genotype

    Sign In

    Description

    Reference Allele

    T

    Alternative Allele

    C

    Chromosome

    9

    Location

    112838568

    Variant Type

    SNP

    Genes

    • SNX30

    Phenotypes

      ClinVar

      © 2024 Biocodify. All rights reserved.

      TwitterTwitter

      Product

      HomePricingDashboard

      DNA

      VariantsGenesPhenotypes

      Stay up to date

      The latest news and updates from Biocodify, sent to your inbox.