rs146292819
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs146292819(G;G) |
Make rs146292819(G;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 104794495 |
Gene | ABCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs146292819 |
dbSNP (classic) | rs146292819 |
ClinGen | rs146292819 |
ebi | rs146292819 |
HLI | rs146292819 |
Exac | rs146292819 |
Gnomad | rs146292819 |
Varsome | rs146292819 |
LitVar | rs146292819 |
Map | rs146292819 |
PheGenI | rs146292819 |
Biobank | rs146292819 |
1000 genomes | rs146292819 |
hgdp | rs146292819 |
ensembl | rs146292819 |
geneview | rs146292819 |
scholar | rs146292819 |
rs146292819 | |
pharmgkb | rs146292819 |
gwascentral | rs146292819 |
openSNP | rs146292819 |
23andMe | rs146292819 |
SNPshot | rs146292819 |
SNPdbe | rs146292819 |
MSV3d | rs146292819 |
GWAS Ctlg | rs146292819 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs146292819(G;G) |
Alt | rs146292819(G;G) |
Reference | Rs146292819(T;T) |
Significance | Pathogenic |
Disease | ABCA1-Related Disorders |
Variation | info |
Gene | ABCA1 |
CLNDBN | ABCA1-Related Disorders |
Reversed | 0 |
HGVS | NC_000009.11:g.107556776T>G |
CLNSRC | Illumina |
CLNACC | RCV000277325.1, |