This variation maps to 7 locations

Select a location:
Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.04 (C)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

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

Variation displays