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rs7118833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs7118833(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position128912107
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs7118833
dbSNP (old)rs7118833
ClinGenrs7118833
ebirs7118833
HLIrs7118833
Exacrs7118833
Gnomadrs7118833
Varsomers7118833
Maprs7118833
PheGenIrs7118833
Biobankrs7118833
1000 genomesrs7118833
hgdprs7118833
ensemblrs7118833
gopubmedrs7118833
geneviewrs7118833
scholarrs7118833
googlers7118833
pharmgkbrs7118833
gwascentralrs7118833
openSNPrs7118833
23andMers7118833
23andMe allrs7118833
SNP Nexus

SNPshotrs7118833
SNPdbers7118833
MSV3drs7118833
GWAS Ctlgrs7118833
GMAF0.163
Max Magnitude0

[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,