This variation maps to 4 locations

Select a location:
Original source

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

Alleles
G/A | Ambiguity code: R
Location

This variation maps to 4 genomic locations; None selected

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays