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rs17176973

From SNPedia

Orientationplus
Stabilizedplus
Make rs17176973(C;C)
Make rs17176973(C;G)
Make rs17176973(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position10811362
is asnp
is mentioned by
dbSNPrs17176973
ebirs17176973
HLIrs17176973
Exacrs17176973
Varsomers17176973
Maprs17176973
PheGenIrs17176973
hapmaprs17176973
1000 genomesrs17176973
hgdprs17176973
ensemblrs17176973
gopubmedrs17176973
geneviewrs17176973
scholarrs17176973
googlers17176973
pharmgkbrs17176973
gwascentralrs17176973
openSNPrs17176973
23andMers17176973
23andMe allrs17176973
SNP Nexus

SNPshotrs17176973
SNPdbers17176973
MSV3drs17176973
GWAS Ctlgrs17176973
GMAF0.01515
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 1.78 [NR]


[PMID 19571809OA-icon.png] Common variants on chromosome 6p22.1 are associated with schizophrenia.