rs147528707
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs147528707(A;A) |
Make rs147528707(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 116790292 |
Gene | APOA5, ZPR1 |
is a | snp |
is | mentioned by |
dbSNP | rs147528707 |
dbSNP (classic) | rs147528707 |
ClinGen | rs147528707 |
ebi | rs147528707 |
HLI | rs147528707 |
Exac | rs147528707 |
Gnomad | rs147528707 |
Varsome | rs147528707 |
LitVar | rs147528707 |
Map | rs147528707 |
PheGenI | rs147528707 |
Biobank | rs147528707 |
1000 genomes | rs147528707 |
hgdp | rs147528707 |
ensembl | rs147528707 |
geneview | rs147528707 |
scholar | rs147528707 |
rs147528707 | |
pharmgkb | rs147528707 |
gwascentral | rs147528707 |
openSNP | rs147528707 |
23andMe | rs147528707 |
SNPshot | rs147528707 |
SNPdbe | rs147528707 |
MSV3d | rs147528707 |
GWAS Ctlg | rs147528707 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147528707(A;A) |
Alt | rs147528707(A;A) |
Reference | Rs147528707(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | APOA5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.116661008G>A |
CLNSRC | |
CLNACC | RCV000478434.1, |