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rs17691888

From SNPedia

Orientationplus
Stabilizedplus
Make rs17691888(A;A)
Make rs17691888(A;G)
Make rs17691888(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position18445599
GeneCACNB2
is asnp
is mentioned by
dbSNPrs17691888
ebirs17691888
HLIrs17691888
Exacrs17691888
Varsomers17691888
Maprs17691888
PheGenIrs17691888
hapmaprs17691888
1000 genomesrs17691888
hgdprs17691888
ensemblrs17691888
gopubmedrs17691888
geneviewrs17691888
scholarrs17691888
googlers17691888
pharmgkbrs17691888
gwascentralrs17691888
openSNPrs17691888
23andMers17691888
23andMe allrs17691888
SNP Nexus

SNPshotrs17691888
SNPdbers17691888
MSV3drs17691888
GWAS Ctlgrs17691888
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23974872OA-icon.png]
Trait Schizophrenia
Title Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Risk Allele G
P-val 1E-10
Odds Ratio 1.16 [1.11-1.21]