rs6590357

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(T;T)	0	common in clinvar

Make rs6590357(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

128911444

Gene	C11orf45, KCNJ5

is a	snp
is	mentioned by
dbSNP	rs6590357
dbSNP (classic)	rs6590357
ClinGen	rs6590357
ebi	rs6590357
HLI	rs6590357
Exac	rs6590357
Gnomad	rs6590357
Varsome	rs6590357
LitVar	rs6590357
Map	rs6590357
PheGenI	rs6590357
Biobank	rs6590357
1000 genomes	rs6590357
hgdp	rs6590357
ensembl	rs6590357
geneview	rs6590357
scholar	rs6590357
google	rs6590357
pharmgkb	rs6590357
gwascentral	rs6590357
openSNP	rs6590357
23andMe	rs6590357
SNPshot	rs6590357
SNPdbe	rs6590357
MSV3d	rs6590357
GWAS Ctlg	rs6590357

GMAF

0.1451

Max Magnitude

0

?

(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 Romano-Ward syndrome Familial hyperaldosteronism
Variation	info
Gene	KCNJ5
CLNDBN	not specified Romano-Ward syndrome Familial hyperaldosteronism
Reversed	0
HGVS	NC_000011.9:g.128781339T>C
CLNSRC	ClinVar GeneDx
CLNACC	RCV000126421.4, RCV000307277.1, RCV000366690.1,