rs724160013
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs724160013(-;GTG) |
Make rs724160013(GTG;GTG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 14097621 |
Gene | PRKACA |
is a | snp |
is | mentioned by |
dbSNP | rs724160013 |
dbSNP (classic) | rs724160013 |
ClinGen | rs724160013 |
ebi | rs724160013 |
HLI | rs724160013 |
Exac | rs724160013 |
Gnomad | rs724160013 |
Varsome | rs724160013 |
LitVar | rs724160013 |
Map | rs724160013 |
PheGenI | rs724160013 |
Biobank | rs724160013 |
1000 genomes | rs724160013 |
hgdp | rs724160013 |
ensembl | rs724160013 |
geneview | rs724160013 |
scholar | rs724160013 |
rs724160013 | |
pharmgkb | rs724160013 |
gwascentral | rs724160013 |
openSNP | rs724160013 |
23andMe | rs724160013 |
SNPshot | rs724160013 |
SNPdbe | rs724160013 |
MSV3d | rs724160013 |
GWAS Ctlg | rs724160013 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs724160013(GTG;GTG) |
Alt | rs724160013(GTG;GTG) |
Reference | Rs724160013(-;-) |
Significance | Pathogenic |
Disease | Pigmented nodular adrenocortical disease |
Variation | info |
Gene | PRKACA |
CLNDBN | Pigmented nodular adrenocortical disease, primary, 4 |
Reversed | 1 |
HGVS | NC_000019.9:g.14208434_14208436dupCAC |
CLNSRC | |
CLNACC | RCV000149856.1, |