Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.40 (C)

Chromosome 7:128954671 (forward strand) | View in location tab


with HGMD-PUBLIC CR068449

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs10373278, rs56657495

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 8 transcripts, has 3764 sample genotypes and is mentioned in 44 citations.

Variant displays