rs2604204
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2604204(A;A) |
Make rs2604204(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 128917535 |
Gene | KCNJ5 |
is a | snp |
is | mentioned by |
dbSNP | rs2604204 |
dbSNP (classic) | rs2604204 |
ClinGen | rs2604204 |
ebi | rs2604204 |
HLI | rs2604204 |
Exac | rs2604204 |
Gnomad | rs2604204 |
Varsome | rs2604204 |
LitVar | rs2604204 |
Map | rs2604204 |
PheGenI | rs2604204 |
Biobank | rs2604204 |
1000 genomes | rs2604204 |
hgdp | rs2604204 |
ensembl | rs2604204 |
geneview | rs2604204 |
scholar | rs2604204 |
rs2604204 | |
pharmgkb | rs2604204 |
gwascentral | rs2604204 |
openSNP | rs2604204 |
23andMe | rs2604204 |
SNPshot | rs2604204 |
SNPdbe | rs2604204 |
MSV3d | rs2604204 |
GWAS Ctlg | rs2604204 |
GMAF | 0.2764 |
Max Magnitude | 0 |
[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, |