Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.27 (A)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs16912051

HGVS name

9:g.122660145G>A

This variation has assays on 6 chips - click the plus to show

Variation displays