rs72981516
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs72981516(G;G) |
Make rs72981516(G;T) |
Make rs72981516(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 72959855 |
Gene | FCHSD2 |
is a | snp |
is | mentioned by |
dbSNP | rs72981516 |
dbSNP (classic) | rs72981516 |
ClinGen | rs72981516 |
ebi | rs72981516 |
HLI | rs72981516 |
Exac | rs72981516 |
Gnomad | rs72981516 |
Varsome | rs72981516 |
LitVar | rs72981516 |
Map | rs72981516 |
PheGenI | rs72981516 |
Biobank | rs72981516 |
1000 genomes | rs72981516 |
hgdp | rs72981516 |
ensembl | rs72981516 |
geneview | rs72981516 |
scholar | rs72981516 |
rs72981516 | |
pharmgkb | rs72981516 |
gwascentral | rs72981516 |
openSNP | rs72981516 |
23andMe | rs72981516 |
SNPshot | rs72981516 |
SNPdbe | rs72981516 |
MSV3d | rs72981516 |
GWAS Ctlg | rs72981516 |
GMAF | 0.04224 |
Max Magnitude | 0 |
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] |