Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H
Location

Chromosome 13:27621426 (forward strand) | View in location tab

Most severe consequence

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 23 transcripts.

Variation displays