Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.47 (C)
Location

Chromosome 22:50568559 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.50568559T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts and has 2776 individual genotypes.

Variation displays