This variation maps to 10 locations

Select a location:
Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

This variation maps to 10 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs635665

HGVS name

None

Variation displays