Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59783909

HGVS names

This variant has 2 HGVS names - Hide

5:g.159391737A>C
ENST00000635333.1:n.283-796A>C

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_ExomeChip

About this variant

This variant overlaps 1 transcript, has 2772 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variant displays