rs2853578
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2853578(A;G) |
Make rs2853578(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 104831027 |
Gene | ABCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs2853578 |
dbSNP (classic) | rs2853578 |
ClinGen | rs2853578 |
ebi | rs2853578 |
HLI | rs2853578 |
Exac | rs2853578 |
Gnomad | rs2853578 |
Varsome | rs2853578 |
LitVar | rs2853578 |
Map | rs2853578 |
PheGenI | rs2853578 |
Biobank | rs2853578 |
1000 genomes | rs2853578 |
hgdp | rs2853578 |
ensembl | rs2853578 |
geneview | rs2853578 |
scholar | rs2853578 |
rs2853578 | |
pharmgkb | rs2853578 |
gwascentral | rs2853578 |
openSNP | rs2853578 |
23andMe | rs2853578 |
SNPshot | rs2853578 |
SNPdbe | rs2853578 |
MSV3d | rs2853578 |
GWAS Ctlg | rs2853578 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs2853578(G;G) |
Alt | rs2853578(G;G) |
Reference | Rs2853578(A;A) |
Significance | Pathogenic |
Disease | Tangier disease |
Variation | info |
Gene | ABCA1 |
CLNDBN | Tangier disease |
Reversed | 1 |
HGVS | NC_000009.11:g.107593308T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000010093.4, |
[PMID 19041386] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.