rs120074112
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs120074112(A;G) |
Make rs120074112(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 44948479 |
Gene | APOC2, APOC4-APOC2 |
is a | snp |
is | mentioned by |
dbSNP | rs120074112 |
dbSNP (classic) | rs120074112 |
ClinGen | rs120074112 |
ebi | rs120074112 |
HLI | rs120074112 |
Exac | rs120074112 |
Gnomad | rs120074112 |
Varsome | rs120074112 |
LitVar | rs120074112 |
Map | rs120074112 |
PheGenI | rs120074112 |
Biobank | rs120074112 |
1000 genomes | rs120074112 |
hgdp | rs120074112 |
ensembl | rs120074112 |
geneview | rs120074112 |
scholar | rs120074112 |
rs120074112 | |
pharmgkb | rs120074112 |
gwascentral | rs120074112 |
openSNP | rs120074112 |
23andMe | rs120074112 |
SNPshot | rs120074112 |
SNPdbe | rs120074112 |
MSV3d | rs120074112 |
GWAS Ctlg | rs120074112 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs120074112(G;G) |
Alt | rs120074112(G;G) |
Reference | Rs120074112(A;A) |
Significance | Pathogenic |
Disease | APOLIPOPROTEIN C-II (PARIS) Apolipoprotein C2 deficiency |
Variation | info |
Gene | APOC2 APOC4-APOC2 |
CLNDBN | APOLIPOPROTEIN C-II (PARIS) Apolipoprotein C2 deficiency |
Reversed | 0 |
HGVS | NC_000019.9:g.45451736A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000002693.2, RCV000002694.2, |