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rs17075286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17075286(C;G)
Make rs17075286(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position43189231
is asnp
is mentioned by
dbSNPrs17075286
ebirs17075286
HLIrs17075286
Exacrs17075286
Varsomers17075286
Maprs17075286
PheGenIrs17075286
hapmaprs17075286
1000 genomesrs17075286
hgdprs17075286
ensemblrs17075286
gopubmedrs17075286
geneviewrs17075286
scholarrs17075286
googlers17075286
pharmgkbrs17075286
gwascentralrs17075286
openSNPrs17075286
23andMers17075286
23andMe allrs17075286
SNP Nexus

SNPshotrs17075286
SNPdbers17075286
MSV3drs17075286
GWAS Ctlgrs17075286
GMAF0.07759
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21057379OA-icon.png]
Trait
Title Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes
Risk Allele
P-val 8E-7
Odds Ratio None None