rs772677312
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs772677312(C;G) |
Make rs772677312(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 55058543 |
Gene | PCSK9 |
is a | snp |
is | mentioned by |
dbSNP | rs772677312 |
dbSNP (classic) | rs772677312 |
ClinGen | rs772677312 |
ebi | rs772677312 |
HLI | rs772677312 |
Exac | rs772677312 |
Gnomad | rs772677312 |
Varsome | rs772677312 |
LitVar | rs772677312 |
Map | rs772677312 |
PheGenI | rs772677312 |
Biobank | rs772677312 |
1000 genomes | rs772677312 |
hgdp | rs772677312 |
ensembl | rs772677312 |
geneview | rs772677312 |
scholar | rs772677312 |
rs772677312 | |
pharmgkb | rs772677312 |
gwascentral | rs772677312 |
openSNP | rs772677312 |
23andMe | rs772677312 |
SNPshot | rs772677312 |
SNPdbe | rs772677312 |
MSV3d | rs772677312 |
GWAS Ctlg | rs772677312 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772677312(G;G) |
Alt | rs772677312(G;G) |
Reference | Rs772677312(C;C) |
Significance | Other |
Disease | Familial hypercholesterolemia |
Variation | info |
Gene | PCSK9 |
CLNDBN | Familial hypercholesterolemia |
Reversed | 0 |
HGVS | NC_000001.10:g.55524216C>G |
CLNSRC | Instituto Nacional de Saúde Doutor Ricardo Jorge |
CLNACC | RCV000256342.1, |