Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.12 (A)

Chromosome 11:116837538 (forward strand) | View in location tab


with HGMD-PUBLIC CR961720

Most severe consequence
5 prime UTR variant
Evidence status


Archive dbSNP rs61758320, rs17249491

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2529 sample genotypes and is mentioned in 5 citations.

Variant displays