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rs4130590

From SNPedia

Orientationplus
Stabilizedplus
Make rs4130590(A;A)
Make rs4130590(A;G)
Make rs4130590(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position127345685
GeneGARNL3
is asnp
is mentioned by
dbSNPrs4130590
ebirs4130590
HLIrs4130590
Exacrs4130590
Varsomers4130590
Maprs4130590
PheGenIrs4130590
hapmaprs4130590
1000 genomesrs4130590
hgdprs4130590
ensemblrs4130590
gopubmedrs4130590
geneviewrs4130590
scholarrs4130590
googlers4130590
pharmgkbrs4130590
gwascentralrs4130590
openSNPrs4130590
23andMers4130590
23andMe allrs4130590
SNP Nexus

SNPshotrs4130590
SNPdbers4130590
MSV3drs4130590
GWAS Ctlgrs4130590
GMAF0.3994
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs4130590
PubMedID [PMID 18711365OA-icon.png]
Condition Bipolar disorder
Gene NR
Risk Allele
pValue 3.00E-006
OR 1.16
95% CI



[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


GET Evidence
rs4130590
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.575
summary