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
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.13 (G)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs52816418, rs57904463

HGVS name

None

This variation has assays on 4 chips - click the plus to show

Variation displays