This variation maps to 7 locations

Select a location:
Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.29 (G)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

This variation has assays on 7 chips - click the plus to show

Variation displays