This variation has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.28 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs60069994, rs34035949

HGVS name

None

This variation has assays on 9 chips - click the plus to show

Variation displays