This variation maps to 8 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: 0.04 (A)
Location

This variation maps to 8 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs116373211, rs116995068

HGVS name

None

This variation has assays on 6 chips - click the plus to show

Variation displays