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
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

This variation has 7 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_ImmunoChip

Variation displays