Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.09 (T)

Chromosome 15:74727108 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs17861105, rs60381661

HGVS name


Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3362 sample genotypes, is associated with 3 phenotypes and is mentioned in 12 citations.

Variant displays