Most severe consequence
24
Upstream gene variant
Alleles
G/T|Ancestral: T|MAF: 0.17 (G)|Highest population MAF: 0.27
Location
Chromosome 18:12779948 (forward strand)|View in location tab
Evidence status 
HGVS name
NC_000018.10:g.12779948G>T
Synonyms
Archive dbSNP rs56547811, rs59359578, rs59874292
Genotyping chips
This variant has assays on 6 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 1 transcript, has 3964 sample genotypes, is associated with 6 phenotypes and is mentioned in 91 citations.
Description from SNPedia
rs2542151 has been reported in a large study to be associated with Crohn's disease.... Show