This variation maps to 7 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 7 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs192285748

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_Human610_Quad, Illumina_HumanOmni5

Variation displays