rs7118824

plus

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

Make rs7118824(G;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

128912083

Gene

KCNJ5

is a	snp
is	mentioned by
dbSNP	rs7118824
dbSNP (classic)	rs7118824
ClinGen	rs7118824
ebi	rs7118824
HLI	rs7118824
Exac	rs7118824
Gnomad	rs7118824
Varsome	rs7118824
LitVar	rs7118824
Map	rs7118824
PheGenI	rs7118824
Biobank	rs7118824
1000 genomes	rs7118824
hgdp	rs7118824
ensembl	rs7118824
geneview	rs7118824
scholar	rs7118824
google	rs7118824
pharmgkb	rs7118824
gwascentral	rs7118824
openSNP	rs7118824
23andMe	rs7118824
SNPshot	rs7118824
SNPdbe	rs7118824
MSV3d	rs7118824
GWAS Ctlg	rs7118824

GMAF

0.1483

Max Magnitude

0

?

(G;G) (G;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

ClinVar
Risk	Rs7118824(G;G)
Alt	Rs7118824(G;G)
Reference	Rs7118824(T;T)
Significance	Non-pathogenic
Disease	not specified Familial hyperaldosteronism Romano-Ward syndrome
Variation	info
Gene	KCNJ5
CLNDBN	not specified Familial hyperaldosteronism Romano-Ward syndrome
Reversed	0
HGVS	NC_000011.9:g.128781978T>G
CLNSRC	ClinVar GeneDx
CLNACC	RCV000126422.4, RCV000330341.1, RCV000389577.1,