Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 22:36281936 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 2841 sample genotypes and is mentioned in 8 citations.

Variant displays