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
C/A/T | Ancestral: C | Ambiguity code: H
Location

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 16 synonyms - click the plus to show

HGVS name

None

Variation displays