chr15:58431476:C>T Detail (hg38) (LIPC)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr15:58,723,675-58,723,675 View the variant detail on this assembly version. |
| hg38 | chr15:58,431,476-58,431,476 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | ||
| Ensemble | ENST00000356113.10:c.-41+325C>T | |
| ENST00000414170.7:c.-40-517C>T |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.509 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:0.383 |
Prediction
ClinVar
| Clinical Significance |
|
| Review star | ![]() |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
|
2004-08-01 | no assertion criteria provided | High density lipoprotein cholesterol level quantitative trait locus 12 |
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.013 | Dyslipidemias | We examined the influence of the promoter polymorphisms -250G/A (rs2070895) and ... | BeFree | 25117371 | Detail |
| 0.042 | coronary artery disease | The common C-480T polymorphism (rs1800588) of the hepatic lipase gene (LIPC) has... | BeFree | 19558527 | Detail |
| 0.024 | Coronary heart disease | The common C-480T polymorphism (rs1800588) of the hepatic lipase gene (LIPC) has... | BeFree | 19558527 | Detail |
| 0.042 | coronary artery disease | A family-based quantitative transmission disequilibrium test (QTDT) revealed sig... | BeFree | 20075193 | Detail |
| 0.008 | Diabetic Nephropathy | [ HL T+ genotypes might increase the risk of developing diabetic nephropathy by ... | GAD | 15983323 | Detail |
| 0.042 | coronary artery disease | We studied this relation by genotyping rs1800588 in the LIPC promoter in a case-... | BeFree | 23874450 | Detail |
| 0.017 | Coronary Arteriosclerosis | The common C-480T polymorphism (rs1800588) of the hepatic lipase gene (LIPC) has... | BeFree | 19558527 | Detail |
| <0.001 | Hashimoto Disease | We analyzed the associations of seven polymorphisms of genes involved in lipid m... | BeFree | 25587205 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NC_000015.10:g.58431476C>T AND High density lipoprotein cholesterol level quantitative trait locus 1... | ClinVar | Detail |
| We examined the influence of the promoter polymorphisms -250G/A (rs2070895) and -514C/T (rs1800588) ... | DisGeNET | Detail |
| The common C-480T polymorphism (rs1800588) of the hepatic lipase gene (LIPC) has been associated wit... | DisGeNET | Detail |
| The common C-480T polymorphism (rs1800588) of the hepatic lipase gene (LIPC) has been associated wit... | DisGeNET | Detail |
| A family-based quantitative transmission disequilibrium test (QTDT) revealed significant association... | DisGeNET | Detail |
| [ HL T+ genotypes might increase the risk of developing diabetic nephropathy by slowing clearance of... | DisGeNET | Detail |
| We studied this relation by genotyping rs1800588 in the LIPC promoter in a case-control study on CAD... | DisGeNET | Detail |
| The common C-480T polymorphism (rs1800588) of the hepatic lipase gene (LIPC) has been associated wit... | DisGeNET | Detail |
| We analyzed the associations of seven polymorphisms of genes involved in lipid metabolism (APOA5 rs3... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs1800588 dbSNP
- Genome
- hg38
- Position
- chr15:58,431,476-58,431,476
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs1800588
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.5086
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 8524
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 8194
- East Asian Allele Counts (ExAC)
- 3141
- East Asian Heterozygous Counts (ExAC)
- 1973
- East Asian Homozygous Counts (ExAC)
- 584
- East Asian Allele Frequency (ExAC)
- 0.38332926531608497
- Chromosome Counts in All Race (ExAC)
- 112760
- Allele Counts in All Race (ExAC)
- 32914
- Heterozygous Counts in All Race (ExAC)
- 21208
- Homozygous Counts in All Race (ExAC)
- 5853
- Allele Frequency in All Race (ExAC)
- 0.2918942887548776
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