Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.09 (G)
Location

Chromosome 11:114057762 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61212963

HGVS name

11:g.114057762A>G

About this variant

This variant overlaps 5 transcripts and has 2574 sample genotypes.

Variant displays