Original source

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

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

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

Co-located variant

HGMD-PUBLIC CR961720

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

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