This variation maps to 7 locations

Select a location:
Original source

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

Alleles
C/G/T | Ambiguity code: B | MAF: 0.12 (T)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 17 synonyms - click the plus to show

HGVS name

None

Variation displays