This variation maps to 2 locations

Select a location:
Original source

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

Alleles
-/T | MAF: 0.06 (T)
Location

This variation maps to 2 genomic locations; None selected

HGVS name

None

Variation displays