This variation maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.02 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

This variation has assays on 4 chips - click the plus to show

Variation displays