This variation maps to 2 locations

Select a location:
Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.43 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs61658810

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni2.5

Variation displays