Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 3761 sample genotypes.

Variant displays