This variation maps to 2 locations

Select a location:
Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.08 (T)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Synonyms

Uniprot VAR_034251

HGVS name

None

This variation has assays on 5 chips - click the plus to show

Variation displays