rs2293889
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs2293889(G;G) |
Make rs2293889(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 115586972 |
Gene | TRPS1 |
is a | snp |
is | mentioned by |
dbSNP | rs2293889 |
dbSNP (classic) | rs2293889 |
ClinGen | rs2293889 |
ebi | rs2293889 |
HLI | rs2293889 |
Exac | rs2293889 |
Gnomad | rs2293889 |
Varsome | rs2293889 |
LitVar | rs2293889 |
Map | rs2293889 |
PheGenI | rs2293889 |
Biobank | rs2293889 |
1000 genomes | rs2293889 |
hgdp | rs2293889 |
ensembl | rs2293889 |
geneview | rs2293889 |
scholar | rs2293889 |
rs2293889 | |
pharmgkb | rs2293889 |
gwascentral | rs2293889 |
openSNP | rs2293889 |
23andMe | rs2293889 |
SNPshot | rs2293889 |
SNPdbe | rs2293889 |
MSV3d | rs2293889 |
GWAS Ctlg | rs2293889 |
GMAF | 0.2525 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20686565![]() |
Trait | |
Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
Risk Allele | T |
P-val | 6E-11 |
Odds Ratio | 0.4400 None |
GWAS snp | |
---|---|
PMID | [PMID 24097068![]() |
Trait | HDL cholesterol |
Title | Discovery and refinement of loci associated with lipid levels. |
Risk Allele | T |
P-val | 4E-17 |
Odds Ratio | .03 [NR] unit decrease |
ClinVar | |
---|---|
Risk | rs2293889(C;C) rs2293889(G;G) |
Alt | rs2293889(C;C) rs2293889(G;G) |
Reference | Rs2293889(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | TRPS1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000008.10:g.116599199T>G |
CLNSRC | |
CLNACC | RCV000249619.1, |
[PMID 30003933] Lipid-associated genetic polymorphisms are associated with FBP and LDL-c levels among myocardial infarction patients in Chinese population.