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rs17166499

From SNPedia

Orientationplus
Stabilizedplus
Make rs17166499(C;C)
Make rs17166499(C;G)
Make rs17166499(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position12897630
is asnp
is mentioned by
dbSNPrs17166499
ebirs17166499
HLIrs17166499
Exacrs17166499
Varsomers17166499
Maprs17166499
PheGenIrs17166499
hapmaprs17166499
1000 genomesrs17166499
hgdprs17166499
ensemblrs17166499
gopubmedrs17166499
geneviewrs17166499
scholarrs17166499
googlers17166499
pharmgkbrs17166499
gwascentralrs17166499
openSNPrs17166499
23andMers17166499
23andMe allrs17166499
SNP Nexus

SNPshotrs17166499
SNPdbers17166499
MSV3drs17166499
GWAS Ctlgrs17166499
GMAF0.129
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 20889312]
Trait Bipolar disorder and schizophrenia
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Risk Allele
P-val 5E-6
Odds Ratio 1.51 [NR]