This variation maps to 3 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
Location

This variation maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs2990222

HGVS name

None

Variation displays