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rs3117099

From SNPedia

Orientationminus
Stabilizedminus
Make rs3117099(C;C)
Make rs3117099(C;T)
Make rs3117099(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32390493
GeneHCG23
is asnp
is mentioned by
dbSNPrs3117099
ebirs3117099
HLIrs3117099
Exacrs3117099
Varsomers3117099
Maprs3117099
PheGenIrs3117099
hapmaprs3117099
1000 genomesrs3117099
hgdprs3117099
ensemblrs3117099
gopubmedrs3117099
geneviewrs3117099
scholarrs3117099
googlers3117099
pharmgkbrs3117099
gwascentralrs3117099
openSNPrs3117099
23andMers3117099
23andMe allrs3117099
SNP Nexus

SNPshotrs3117099
SNPdbers3117099
MSV3drs3117099
GWAS Ctlgrs3117099
GMAF0.314
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22688191OA-icon.png]
Trait
Title Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Risk Allele
P-val 0.000003
Odds Ratio 1.2500 None


[PMID 17927685] BTNL2 allele associations with chronic beryllium disease in HLA-DPB1*Glu69-negative individuals.


[PMID 18204098] Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.


[PMID 20018075OA-icon.png] Genome-wide association study of rheumatoid arthritis by a score test based on wavelet transformation.