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rs6590357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs6590357(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position128911444
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs6590357
ebirs6590357
HLIrs6590357
Exacrs6590357
Varsomers6590357
Maprs6590357
PheGenIrs6590357
hapmaprs6590357
1000 genomesrs6590357
hgdprs6590357
ensemblrs6590357
gopubmedrs6590357
geneviewrs6590357
scholarrs6590357
googlers6590357
pharmgkbrs6590357
gwascentralrs6590357
openSNPrs6590357
23andMers6590357
23andMe allrs6590357
SNP Nexus

SNPshotrs6590357
SNPdbers6590357
MSV3drs6590357
GWAS Ctlgrs6590357
GMAF0.1451
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19208499] The single nucleotide polymorphisms of Kir3.4 gene and their correlation with lone paroxysmal atrial fibrillation in Chinese Han population


[PMID 21555883] Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians


[PMID 22645387] Influence of age on the association of GIRK4 with metabolic syndrome.


[PMID 24382237] Relationship between the G Protein Gated Inward Rectifier Potassium Channel 4 Gene Polymorphism and Dyslipidemia of Uyghur Residents


ClinVar
Risk rs6590357(C;C)
Alt rs6590357(C;C)
Reference rs6590357(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene KCNJ5
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.128781339T>C
CLNSRC ClinVar GeneDx
CLNACC RCV000126421.3,