rs11673492
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs11673492(C;T) |
Make rs11673492(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 40714624 |
Gene | COQ8B |
is a | snp |
is | mentioned by |
dbSNP | rs11673492 |
dbSNP (classic) | rs11673492 |
ClinGen | rs11673492 |
ebi | rs11673492 |
HLI | rs11673492 |
Exac | rs11673492 |
Gnomad | rs11673492 |
Varsome | rs11673492 |
LitVar | rs11673492 |
Map | rs11673492 |
PheGenI | rs11673492 |
Biobank | rs11673492 |
1000 genomes | rs11673492 |
hgdp | rs11673492 |
ensembl | rs11673492 |
geneview | rs11673492 |
scholar | rs11673492 |
rs11673492 | |
pharmgkb | rs11673492 |
gwascentral | rs11673492 |
openSNP | rs11673492 |
23andMe | rs11673492 |
SNPshot | rs11673492 |
SNPdbe | rs11673492 |
MSV3d | rs11673492 |
GWAS Ctlg | rs11673492 |
GMAF | 0.1267 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24621571] Single-Nucleotide Polymorphism rs7251246 in ITPKC Is Associated with Susceptibility and Coronary Artery Lesions in Kawasaki Disease
ClinVar | |
---|---|
Risk | rs11673492(T;T) |
Alt | rs11673492(T;T) |
Reference | Rs11673492(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | COQ8B ADCK4 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000019.9:g.41220529C>T |
CLNSRC | |
CLNACC | RCV000432894.1, |