rs11861007
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11861007(C;C) |
Make rs11861007(C;T) |
Make rs11861007(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 79204788 |
Gene | MAF, WWOX |
is a | snp |
is | mentioned by |
dbSNP | rs11861007 |
dbSNP (classic) | rs11861007 |
ClinGen | rs11861007 |
ebi | rs11861007 |
HLI | rs11861007 |
Exac | rs11861007 |
Gnomad | rs11861007 |
Varsome | rs11861007 |
LitVar | rs11861007 |
Map | rs11861007 |
PheGenI | rs11861007 |
Biobank | rs11861007 |
1000 genomes | rs11861007 |
hgdp | rs11861007 |
ensembl | rs11861007 |
geneview | rs11861007 |
scholar | rs11861007 |
rs11861007 | |
pharmgkb | rs11861007 |
gwascentral | rs11861007 |
openSNP | rs11861007 |
23andMe | rs11861007 |
SNPshot | rs11861007 |
SNPdbe | rs11861007 |
MSV3d | rs11861007 |
GWAS Ctlg | rs11861007 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 29361163] Genomic and expression analyses identify a disease modifying variant for fibrostenotic Crohn's disease.