This variation maps to 3 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/C | Ancestral: G | Ambiguity code: V | MAF: 0.02 (C)
Location

This variation maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs34569076

HGVS name

None

Variation displays