Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58850559

HGVS names

This variant has 2 HGVS names - Hide

5:g.159395637G>C
ENST00000635333.1:n.327+3060G>C

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 transcript, has 4208 sample genotypes, is associated with 1 phenotype and is mentioned in 66 citations.

Variant displays