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rs17040430

From SNPedia

Orientationplus
Stabilizedplus
Make rs17040430(G;G)
Make rs17040430(G;T)
Make rs17040430(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position108349043
is asnp
is mentioned by
dbSNPrs17040430
ebirs17040430
HLIrs17040430
Exacrs17040430
Varsomers17040430
Maprs17040430
PheGenIrs17040430
hapmaprs17040430
1000 genomesrs17040430
hgdprs17040430
ensemblrs17040430
gopubmedrs17040430
geneviewrs17040430
scholarrs17040430
googlers17040430
pharmgkbrs17040430
gwascentralrs17040430
openSNPrs17040430
23andMers17040430
23andMe allrs17040430
SNP Nexus

SNPshotrs17040430
SNPdbers17040430
MSV3drs17040430
GWAS Ctlgrs17040430
GMAF0.03857
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22688191OA-icon.png]
Trait
Title Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Risk Allele T
P-val 9E-7
Odds Ratio 1.8900 None