Have questions? Visit https://www.reddit.com/r/SNPedia

rs72981516

From SNPedia

Orientationplus
Stabilizedplus
Make rs72981516(G;G)
Make rs72981516(G;T)
Make rs72981516(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position72959855
GeneFCHSD2
is asnp
is mentioned by
dbSNPrs72981516
ebirs72981516
HLIrs72981516
Exacrs72981516
Varsomers72981516
Maprs72981516
PheGenIrs72981516
hapmaprs72981516
1000 genomesrs72981516
hgdprs72981516
ensemblrs72981516
gopubmedrs72981516
geneviewrs72981516
scholarrs72981516
googlers72981516
pharmgkbrs72981516
gwascentralrs72981516
openSNPrs72981516
23andMers72981516
23andMe allrs72981516
SNP Nexus

SNPshotrs72981516
SNPdbers72981516
MSV3drs72981516
GWAS Ctlgrs72981516
GMAF0.04224
Max Magnitude
GWAS snp
PMID [PMID 23266558]
Trait Crohn's disease
Title A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
Risk Allele T
P-val 4E-7
Odds Ratio 1.28 [1.27-1.29]