This variation maps to 5 locations

Select a location:
Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: 0.17 (T)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

This variation has 5 synonyms - click the plus to show

HGVS name

None

Variation displays