Have questions? Visit https://www.reddit.com/r/SNPedia

rs17746001

From SNPedia

Orientationplus
Stabilizedplus
Make rs17746001(C;C)
Make rs17746001(C;T)
Make rs17746001(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position179734472
is asnp
is mentioned by
dbSNPrs17746001
ebirs17746001
HLIrs17746001
Exacrs17746001
Varsomers17746001
Maprs17746001
PheGenIrs17746001
hapmaprs17746001
1000 genomesrs17746001
hgdprs17746001
ensemblrs17746001
gopubmedrs17746001
geneviewrs17746001
scholarrs17746001
googlers17746001
pharmgkbrs17746001
gwascentralrs17746001
openSNPrs17746001
23andMers17746001
23andMe allrs17746001
SNP Nexus

SNPshotrs17746001
SNPdbers17746001
MSV3drs17746001
GWAS Ctlgrs17746001
GMAF0.05739
Max Magnitude
? (C;C) (C;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 3E-7
Odds Ratio 1.7500 None