Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (T)

Chromosome 12:21635266 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays