Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.21 (C)

Chromosome 10:113029056 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17685444, rs60689663

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 15 transcripts, 2 regulatory features, has 3996 sample genotypes, is associated with 3 phenotypes and is mentioned in 10 citations.

Variant displays