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rs11210359

From SNPedia

Orientationplus
Stabilizedplus
Make rs11210359(A;A)
Make rs11210359(A;G)
Make rs11210359(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position73873484
is asnp
is mentioned by
dbSNPrs11210359
ebirs11210359
HLIrs11210359
Exacrs11210359
Varsomers11210359
Maprs11210359
PheGenIrs11210359
hapmaprs11210359
1000 genomesrs11210359
hgdprs11210359
ensemblrs11210359
gopubmedrs11210359
geneviewrs11210359
scholarrs11210359
googlers11210359
pharmgkbrs11210359
gwascentralrs11210359
openSNPrs11210359
23andMers11210359
23andMe allrs11210359
SNP Nexus

SNPshotrs11210359
SNPdbers11210359
MSV3drs11210359
GWAS Ctlgrs11210359
GMAF0.3522
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000008
Odds Ratio None None