rs2061634
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2061634(C;C) |
Make rs2061634(C;G) |
Make rs2061634(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 97343500 |
Gene | CCDC180, LOC100499484-C9ORF174 |
is a | snp |
is | mentioned by |
dbSNP | rs2061634 |
dbSNP (classic) | rs2061634 |
ClinGen | rs2061634 |
ebi | rs2061634 |
HLI | rs2061634 |
Exac | rs2061634 |
Gnomad | rs2061634 |
Varsome | rs2061634 |
LitVar | rs2061634 |
Map | rs2061634 |
PheGenI | rs2061634 |
Biobank | rs2061634 |
1000 genomes | rs2061634 |
hgdp | rs2061634 |
ensembl | rs2061634 |
geneview | rs2061634 |
scholar | rs2061634 |
rs2061634 | |
pharmgkb | rs2061634 |
gwascentral | rs2061634 |
openSNP | rs2061634 |
23andMe | rs2061634 |
SNPshot | rs2061634 |
SNPdbe | rs2061634 |
MSV3d | rs2061634 |
GWAS Ctlg | rs2061634 |
GMAF | 0.2479 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 19442274] First genome-wide association study for this disorder, albeit of 152 patients, reports an association between this SNP (odds ratio 2.04, p = 4.2 x10e-5) and Behcet's disease.