Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.15 (A)
Location

Chromosome 5:159387525 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs11135060, rs59372928

HGVS names

This variant has 2 HGVS names - Hide

5:g.159387525A>C
ENST00000635333.1:n.283-5008A>C

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 1 transcript, has 3615 sample genotypes, is associated with 2 phenotypes and is mentioned in 25 citations.

Variant displays