rs1736148
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1736148(C;C) |
Make rs1736148(C;T) |
Make rs1736148(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 15440893 |
Gene | LOC101927745 |
is a | snp |
is | mentioned by |
dbSNP | rs1736148 |
dbSNP (classic) | rs1736148 |
ClinGen | rs1736148 |
ebi | rs1736148 |
HLI | rs1736148 |
Exac | rs1736148 |
Gnomad | rs1736148 |
Varsome | rs1736148 |
LitVar | rs1736148 |
Map | rs1736148 |
PheGenI | rs1736148 |
Biobank | rs1736148 |
1000 genomes | rs1736148 |
hgdp | rs1736148 |
ensembl | rs1736148 |
geneview | rs1736148 |
scholar | rs1736148 |
rs1736148 | |
pharmgkb | rs1736148 |
gwascentral | rs1736148 |
openSNP | rs1736148 |
23andMe | rs1736148 |
SNPshot | rs1736148 |
SNPdbe | rs1736148 |
MSV3d | rs1736148 |
GWAS Ctlg | rs1736148 |
GMAF | 0.3926 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
DeCode reports that rs1736148 is associated with susceptibility to Crohn's disease. [PMID 18587394]