rs7118833

plus

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

Make rs7118833(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

128912107

Gene

KCNJ5

is a	snp
is	mentioned by
dbSNP	rs7118833
dbSNP (classic)	rs7118833
ClinGen	rs7118833
ebi	rs7118833
HLI	rs7118833
Exac	rs7118833
Gnomad	rs7118833
Varsome	rs7118833
LitVar	rs7118833
Map	rs7118833
PheGenI	rs7118833
Biobank	rs7118833
1000 genomes	rs7118833
hgdp	rs7118833
ensembl	rs7118833
geneview	rs7118833
scholar	rs7118833
google	rs7118833
pharmgkb	rs7118833
gwascentral	rs7118833
openSNP	rs7118833
23andMe	rs7118833
SNPshot	rs7118833
SNPdbe	rs7118833
MSV3d	rs7118833
GWAS Ctlg	rs7118833

GMAF

0.163

Max Magnitude

0

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

ClinVar
Risk	Rs7118833(C;C)
Alt	Rs7118833(C;C)
Reference	Rs7118833(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.128782002T>C
CLNSRC	ClinVar GeneDx
CLNACC	RCV000126423.4, RCV000295128.1, RCV000345335.1,