Most severe consequence
21
Intron variant
Alleles
A/G|Ancestral: A|MAF: 0.14 (G)|Highest population MAF: 0.49
Location
Chromosome 12:112049014 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
Archive dbSNP rs60107056
Genotyping chips
This variant has assays on 14 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 4 transcripts, has 3531 sample genotypes, is associated with 5 phenotypes and is mentioned in 47 citations.
Description from SNPedia
rs17696736 has been reported in a large study to be associated with type-1 diabetes.... Show