Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (T)

Chromosome 10:99531610 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts and has 2508 sample genotypes.

Variant displays