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rs7799181

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7799181(A;G)
Make rs7799181(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position146351738
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs7799181
ebirs7799181
HLIrs7799181
Exacrs7799181
Varsomers7799181
Maprs7799181
PheGenIrs7799181
hapmaprs7799181
1000 genomesrs7799181
hgdprs7799181
ensemblrs7799181
gopubmedrs7799181
geneviewrs7799181
scholarrs7799181
googlers7799181
pharmgkbrs7799181
gwascentralrs7799181
openSNPrs7799181
23andMers7799181
23andMe allrs7799181
SNP Nexus

SNPshotrs7799181
SNPdbers7799181
MSV3drs7799181
GWAS Ctlgrs7799181
GMAF0.0877
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20889312]
Trait
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder
Risk Allele C
P-val 0.000002
Odds Ratio 2.26 [NR]