Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.07 (C)
Location

Chromosome 9:22003791 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 18 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 19 transcripts, has 3599 sample genotypes and is mentioned in 2 citations.

Variant displays