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
A/G/T | Ambiguity code: D | MAF: 0.21 (G)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 12 synonyms - click the plus to show

HGVS name

None

Variation displays