Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.35 (T)

Chromosome 10:31528977 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs52825274, rs18841, rs58911991

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 3612 sample genotypes and is mentioned in 5 citations.

Variant displays