Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.41 (C)
Location

Chromosome 5:159395637 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs58850559

HGVS name

5:g.159395637G>C

This variant has assays on 5 chips - click the plus to show

About this variant

This variant has 2684 sample genotypes, is associated with 1 phenotype and is mentioned in 64 citations.

Variant displays