rs8111071
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | normal |
(A;G) | 1.5x risk | |
(G;G) | 1.3x risk |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 45804148 |
Gene | RSPH6A |
is a | snp |
is | mentioned by |
dbSNP | rs8111071 |
dbSNP (classic) | rs8111071 |
ClinGen | rs8111071 |
ebi | rs8111071 |
HLI | rs8111071 |
Exac | rs8111071 |
Gnomad | rs8111071 |
Varsome | rs8111071 |
LitVar | rs8111071 |
Map | rs8111071 |
PheGenI | rs8111071 |
Biobank | rs8111071 |
1000 genomes | rs8111071 |
hgdp | rs8111071 |
ensembl | rs8111071 |
geneview | rs8111071 |
scholar | rs8111071 |
rs8111071 | |
pharmgkb | rs8111071 |
gwascentral | rs8111071 |
openSNP | rs8111071 |
23andMe | rs8111071 |
SNPshot | rs8111071 |
SNPdbe | rs8111071 |
MSV3d | rs8111071 |
GWAS Ctlg | rs8111071 |
GMAF | 0.03168 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
rs8111071 has been reported in a large study to be associated with Crohn's disease.
The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.47 (CI 1.25-1.73), and for homozygotes, 1.28 (CI 0.56-2.88). [PMID 17554300]
GWAS snp | |
---|---|
PMID | [PMID 21658281] |
Trait | |
Title | GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. |
Risk Allele | |
P-val | 0.000004 |
Odds Ratio | 2.0100 [1.50-2.70] |
[PMID 20018022] Replication of recently identified associated single-nucleotide polymorphisms from six autoimmune diseases in Genetic Analysis Workshop 16 rheumatoid arthritis data.