Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.29 (A)
Location

Chromosome 9:122660145 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs16912051

HGVS name

9:g.122660145G>A

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3761 sample genotypes.

Variant displays