This variation maps to 2 locations

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: 0.01 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

Uniprot VAR_065082

HGVS name

None

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

Variation displays