This variation maps to 9 locations

Select a location:
Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.36 (G)
Location

This variation maps to 9 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs17305297

HGVS name

None

Variation displays