rs11190141
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11190141(C;C) |
Make rs11190141(C;T) |
Make rs11190141(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 99532633 |
Gene | LINC01475, NKX2-3 |
is a | snp |
is | mentioned by |
dbSNP | rs11190141 |
dbSNP (classic) | rs11190141 |
ClinGen | rs11190141 |
ebi | rs11190141 |
HLI | rs11190141 |
Exac | rs11190141 |
Gnomad | rs11190141 |
Varsome | rs11190141 |
LitVar | rs11190141 |
Map | rs11190141 |
PheGenI | rs11190141 |
Biobank | rs11190141 |
1000 genomes | rs11190141 |
hgdp | rs11190141 |
ensembl | rs11190141 |
geneview | rs11190141 |
scholar | rs11190141 |
rs11190141 | |
pharmgkb | rs11190141 |
gwascentral | rs11190141 |
openSNP | rs11190141 |
23andMe | rs11190141 |
SNPshot | rs11190141 |
SNPdbe | rs11190141 |
MSV3d | rs11190141 |
GWAS Ctlg | rs11190141 |
GMAF | 0.4275 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 22412388![]() |
Trait | |
Title | A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. |
Risk Allele | C |
P-val | 5E-7 |
Odds Ratio | 1.3400 None |