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
A/T | Ancestral: T | Ambiguity code: W
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs3810802

HGVS name

None

Variation displays