This variation has been flagged

Flagged as suspect by dbSNP

Select a location:
Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

This variation maps to 7 genomic locations; None selected

Evidence status

HGVS name

None

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

Variation displays