Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.17 (A)
Location

Chromosome 5:159391737 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs59783909

HGVS name

5:g.159391737A>C

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_ExomeChip

About this variant

This variant has 2535 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays