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rs11720452

From SNPedia

Orientationplus
Stabilizedplus
Make rs11720452(C;C)
Make rs11720452(C;T)
Make rs11720452(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position21207150
is asnp
is mentioned by
dbSNPrs11720452
ebirs11720452
HLIrs11720452
Exacrs11720452
Varsomers11720452
Maprs11720452
PheGenIrs11720452
hapmaprs11720452
1000 genomesrs11720452
hgdprs11720452
ensemblrs11720452
gopubmedrs11720452
geneviewrs11720452
scholarrs11720452
googlers11720452
pharmgkbrs11720452
gwascentralrs11720452
openSNPrs11720452
23andMers11720452
23andMe allrs11720452
SNP Nexus

SNPshotrs11720452
SNPdbers11720452
MSV3drs11720452
GWAS Ctlgrs11720452
GMAF0.1763
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18711365OA-icon.png]
Trait Bipolar disorder
Title Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Risk Allele
P-val 0.0000050000000000000004
Odds Ratio 1.15 [NR]


[PMID 20386566] Genome-wide association study of bipolar I disorder in the Han Chinese population.


GET Evidence
rs11720452
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.195312
summary