Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.06 (G)
Location

Chromosome 1:12269332 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs9430688, rs17880034

HGVS name

1:g.12269332A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5

Variation displays