Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 22:51066990 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.51066990C>T

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni2.5

Variation displays