Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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 2522 sample genotypes.

Variant displays