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rs8111071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 normal
(A;G) 1.5x risk
(G;G) 1.3x risk
ReferenceGRCh38 38.1/141
Chromosome19
Position45804148
GeneRSPH6A
is asnp
is mentioned by
dbSNPrs8111071
dbSNP (classic)rs8111071
ClinGenrs8111071
ebirs8111071
HLIrs8111071
Exacrs8111071
Gnomadrs8111071
Varsomers8111071
LitVarrs8111071
Maprs8111071
PheGenIrs8111071
Biobankrs8111071
1000 genomesrs8111071
hgdprs8111071
ensemblrs8111071
geneviewrs8111071
scholarrs8111071
googlers8111071
pharmgkbrs8111071
gwascentralrs8111071
openSNPrs8111071
23andMers8111071
SNPshotrs8111071
SNPdbers8111071
MSV3drs8111071
GWAS Ctlgrs8111071
GMAF0.03168
Max Magnitude0
? (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 17554300OA-icon.png]

GWAS snp
PMID [PMID 21658281OA-icon.png]
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 20018022OA-icon.png] Replication of recently identified associated single-nucleotide polymorphisms from six autoimmune diseases in Genetic Analysis Workshop 16 rheumatoid arthritis data.