Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)
Location

Chromosome 13:48232482 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.48232482A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2504 individual genotypes.

Variation displays