This variation has been flagged

Variation maps to 2 genomic locations

Select a location:
Original source

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

Alleles
G/T | Ambiguity code: K
Location

This variation maps to 2 genomic locations; None selected

Synonyms

Archive dbSNP rs2621709

HGVS name

None

Variation displays