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rs10911902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs10911902(C;T)
Make rs10911902(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position186663185
is asnp
is mentioned by
dbSNPrs10911902
ebirs10911902
HLIrs10911902
Exacrs10911902
Varsomers10911902
Maprs10911902
PheGenIrs10911902
hapmaprs10911902
1000 genomesrs10911902
hgdprs10911902
ensemblrs10911902
gopubmedrs10911902
geneviewrs10911902
scholarrs10911902
googlers10911902
pharmgkbrs10911902
gwascentralrs10911902
openSNPrs10911902
23andMers10911902
23andMe allrs10911902
SNP Nexus

SNPshotrs10911902
SNPdbers10911902
MSV3drs10911902
GWAS Ctlgrs10911902
GMAF0.1203
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10911902
PubMedID [PMID 18347602OA-icon.png]
Condition Schizophrenia
Gene Intergenic
Risk Allele
pValue 2.00E-006
OR 1.79
95% CI



[PMID 18768181OA-icon.png] Association of polymorphisms in cyclooxygenase (COX)-2 with coronary and carotid calcium in the Diabetes Heart Study.


GET Evidence
rs10911902
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary