Original source

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

Alleles
T/C | Ambiguity code: Y | MAF: 0.15 (C)
Location

Chromosome 22:19152050 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs9618490

HGVS name

22:g.19152050T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2508 individual genotypes.

Variation displays