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rs1170612

From SNPedia

Orientationplus
Stabilizedplus
Make rs1170612(C;C)
Make rs1170612(C;T)
Make rs1170612(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position124225479
GeneCNTNAP5
is asnp
is mentioned by
dbSNPrs1170612
ebirs1170612
HLIrs1170612
Exacrs1170612
Varsomers1170612
Maprs1170612
PheGenIrs1170612
hapmaprs1170612
1000 genomesrs1170612
hgdprs1170612
ensemblrs1170612
gopubmedrs1170612
geneviewrs1170612
scholarrs1170612
googlers1170612
pharmgkbrs1170612
gwascentralrs1170612
openSNPrs1170612
23andMers1170612
23andMe allrs1170612
SNP Nexus

SNPshotrs1170612
SNPdbers1170612
MSV3drs1170612
GWAS Ctlgrs1170612
GMAF0.1534
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22885689]
Trait Schizophrenia
Title Genome-wide association study of multiplex schizophrenia pedigrees.
Risk Allele
P-val 9E-6
Odds Ratio 1.37 [NR]