This variation maps to 5 locations

Select a location:
Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.07 (T)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs115012998, rs118132438

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays