This variation maps to 2 locations

Select a location:
Original source

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

Alleles
A/C/G/T | Ambiguity code: N | MAF: 0.17 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

This variation has 4 synonyms - click the plus to show

HGVS name

None

Variation displays