Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.50 (T)

Chromosome 11:120792654 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17245727, rs60428773

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3764 sample genotypes and is mentioned in 20 citations.

Variant displays