Original source

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

G/A|Ancestral: A|Ambiguity code: R|MAF: 0.43 (G)

Chromosome 11:119088621 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60012314, rs56459440

HGVS names

This variant has 46 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 50 transcripts, 1 regulatory feature, has 3699 sample genotypes and is mentioned in 1 citation.

Variant displays