rs6136
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common |
(A;C) | None | |
(C;C) | None | |
(T;T) | 0 |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 169594713 |
Gene | SELP |
is a | snp |
is | mentioned by |
dbSNP | rs6136 |
dbSNP (classic) | rs6136 |
ClinGen | rs6136 |
ebi | rs6136 |
HLI | rs6136 |
Exac | rs6136 |
Gnomad | rs6136 |
Varsome | rs6136 |
LitVar | rs6136 |
Map | rs6136 |
PheGenI | rs6136 |
Biobank | rs6136 |
1000 genomes | rs6136 |
hgdp | rs6136 |
ensembl | rs6136 |
geneview | rs6136 |
scholar | rs6136 |
rs6136 | |
pharmgkb | rs6136 |
gwascentral | rs6136 |
openSNP | rs6136 |
23andMe | rs6136 |
SNPshot | rs6136 |
SNPdbe | rs6136 |
MSV3d | rs6136 |
GWAS Ctlg | rs6136 |
GMAF | 0.04408 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 17944986] cardiovascular risk
GWAS snp | |
---|---|
PMID | [PMID 20167578] |
Trait | Soluble levels of adhesion molecules |
Title | Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels |
Risk Allele | T |
P-val | 4E-61 |
Odds Ratio | 22.60 [19.86-25.34] % increase |
[PMID 22473907] P-selectin genotype is associated with the development of cancer cachexia
ClinVar | |
---|---|
Risk | Rs6136(C;C) |
Alt | Rs6136(C;C) |
Reference | Rs6136(A;A) |
Significance | Non-pathogenic |
Disease | SELECTIN P POLYMORPHISM |
Variation | info |
Gene | SELP |
CLNDBN | SELECTIN P POLYMORPHISM |
Reversed | 1 |
HGVS | NC_000001.10:g.169563951T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014482.2, |
[PMID 16820586] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.
[PMID 19404301] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.
[PMID 24504449] SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis
[PMID 25147926] Cellular Adhesion Gene SELP Is Associated with Rheumatoid Arthritis and Displays Differential Allelic Expression
[PMID 30047017] Association of SELP Polymorphisms with Soluble P-Selectin Levels and Vascular Risk in Patients with Type 2 Diabetes Mellitus: A Case-Control Study.