Original source

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

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

Chromosome 1:12209275 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs9430688, rs17880034

HGVS name

1:g.12209275A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_1M-duo

Variation displays