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rs17645023

From SNPedia

Orientationplus
Stabilizedplus
Make rs17645023(A;A)
Make rs17645023(A;T)
Make rs17645023(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position66920916
is asnp
is mentioned by
dbSNPrs17645023
ebirs17645023
HLIrs17645023
Exacrs17645023
Varsomers17645023
Maprs17645023
PheGenIrs17645023
hapmaprs17645023
1000 genomesrs17645023
hgdprs17645023
ensemblrs17645023
gopubmedrs17645023
geneviewrs17645023
scholarrs17645023
googlers17645023
pharmgkbrs17645023
gwascentralrs17645023
openSNPrs17645023
23andMers17645023
23andMe allrs17645023
SNP Nexus

SNPshotrs17645023
SNPdbers17645023
MSV3drs17645023
GWAS Ctlgrs17645023
GMAF0.2498
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 21057379OA-icon.png]
Trait
Title Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes
Risk Allele
P-val 6E-7
Odds Ratio None None


[PMID 27102562] Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia.