This variation maps to 7 locations

Select a location:
Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.11 (A)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 10 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5, Illumina_ImmunoChip

Variation displays