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rs2604204

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2604204(A;A)
Make rs2604204(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position128917535
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs2604204
dbSNP (old)rs2604204
ClinGenrs2604204
ebirs2604204
HLIrs2604204
Exacrs2604204
Varsomers2604204
Maprs2604204
PheGenIrs2604204
Biobankrs2604204
1000 genomesrs2604204
hgdprs2604204
ensemblrs2604204
gopubmedrs2604204
geneviewrs2604204
scholarrs2604204
googlers2604204
pharmgkbrs2604204
gwascentralrs2604204
openSNPrs2604204
23andMers2604204
23andMe allrs2604204
SNP Nexus

SNPshotrs2604204
SNPdbers2604204
MSV3drs2604204
GWAS Ctlgrs2604204
GMAF0.2764
Max Magnitude0

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


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


ClinVar
Risk rs2604204(A;A)
Alt rs2604204(A;A)
Reference Rs2604204(C;C)
Significance Non-pathogenic
Disease Romano-Ward syndrome Familial hyperaldosteronism
Variation info
Gene KCNJ5
CLNDBN Romano-Ward syndrome Familial hyperaldosteronism
Reversed 1
HGVS NC_000011.9:g.128787430G>T
CLNSRC
CLNACC RCV000296511.1, RCV000344397.1,