chr15:58702768:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr15:58,702,768-58,862,043
hg38 chr15:58,410,569-58,569,844 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.013 Cardiovascular Diseases NA BeFree,GAD Detail
0.003 Carotid Artery Diseases NA LHGDN Detail
0.003 carotid stenosis NA BeFree,GAD Detail
0.002 cerebral infarction NA GAD Detail
0.002 chorioamnionitis NA GAD Detail
<0.001 colorectal carcinoma NA BeFree Detail
0.017 Coronary Arteriosclerosis NA BeFree,GAD Detail
0.024 Coronary heart disease NA BeFree,GAD Detail
0.001 Diabetes NA BeFree Detail
0.006 diabetes mellitus NA BeFree,GAD,LHGDN Detail
0.080 Diabetes Mellitus, Experimental NA RGD Detail
<0.001 Diabetes Mellitus, Insulin-Dependent NA BeFree Detail
0.275 Diabetes Mellitus, Non-Insulin-Dependent NA BeFree,CLINVAR,CTD_human,GAD Detail
0.008 Diabetic Nephropathy NA GAD,LHGDN Detail
0.002 patent ductus arteriosus NA GAD Detail
<0.001 endometriosis Lack of association between LIPC-514 C/T polymorphism of hepatic lipase and endo... BeFree 24124978 Detail
0.002 Fatty Liver NA GAD Detail
0.080 Fetal Macrosomia NA RGD Detail
0.002 Fetal Membranes, Premature Rupture NA GAD Detail
0.002 generalized atherosclerosis NA GAD Detail
0.080 Focal glomerulosclerosis NA RGD Detail
0.002 Heart Diseases NA GAD Detail
0.080 hepatitis NA RGD Detail
0.002 HIV Infections NA GAD Detail
0.097 Hypercholesterolemia NA BeFree,GAD,RGD Detail
0.121 Hypercholesterolemia, Familial NA BeFree,CTD_human Detail
0.122 Hyperemia NA CTD_human,GAD Detail
0.080 hyperinsulinism NA RGD Detail
0.214 Hyperlipidemia NA CTD_human,GAD,RGD Detail
0.001 Hyperlipidemia, Familial Combined NA BeFree Detail
0.205 Hyperlipoproteinemias NA CTD_human,GAD,RGD Detail
0.002 hyperlipoproteinemia type III NA GAD Detail
0.013 Hypertensive disease Variants -250G/A and -514C/T in the LIPC gene are associated with hypertensive d... BeFree,GAD,LHGDN 25117371 Detail
0.005 Hypertriglyceridemia NA GAD Detail
0.080 Hypoproteinemia NA RGD Detail
0.080 hypothyroidism NA RGD Detail
0.001 hypotrichosis NA BeFree Detail
0.002 Inflammation NA GAD Detail
0.080 ischemia NA RGD Detail
0.003 Kidney Diseases NA BeFree,GAD Detail
0.082 Kidney Failure, Chronic NA GAD,RGD Detail
0.002 Premature Obstetric Labor NA GAD Detail
0.120 Lipid Metabolism, Inborn Errors NA CTD_human Detail
0.002 Chronic Obstructive Airway Disease NA GAD Detail
0.002 Lymphoma, Non-Hodgkin NA GAD Detail
0.018 myocardial infarction NA BeFree,GAD,LHGDN Detail
0.080 nephrotic syndrome NA RGD Detail
0.103 obesity NA BeFree,GAD,RGD Detail
0.010 pre-eclampsia NA GAD,LHGDN Detail
0.080 protein-energy malnutrition NA RGD Detail
0.007 Cerebrovascular accident NA BeFree,GAD Detail
0.003 Vascular Diseases NA LHGDN Detail
0.010 Peripheral Vascular Diseases NA BeFree,GAD,LHGDN Detail
0.003 colorectal cancer Ten non-synonymous single nucleotide polymorphisms (nsSNPs), which were recently... BeFree 18619730 Detail
<0.001 colorectal carcinoma Ten non-synonymous single nucleotide polymorphisms (nsSNPs), which were recently... BeFree 18619730 Detail
0.003 Sudden cardiac death NA LHGDN Detail
0.002 Premature Birth NA GAD Detail
0.007 Myocardial Ischemia NA BeFree,GAD Detail
0.003 Lipid Metabolism Disorders NA BeFree,GAD Detail
0.003 Malignant neoplasm of lung NA BeFree,GAD Detail
0.080 Sepsis NA RGD Detail
<0.001 Impaired glucose tolerance NA BeFree Detail
<0.001 Obesity, Abdominal NA BeFree Detail
0.002 Restenosis NA GAD Detail
0.002 Complications of Diabetes Mellitus NA GAD Detail
0.001 Cholesteryl Ester Transfer Protein Deficiency NA BeFree Detail
0.001 Wooly hair NA BeFree Detail
0.002 Cardiac Death NA GAD Detail
0.002 dementia NA GAD Detail
<0.001 Overweight NA BeFree Detail
0.002 body mass NA GAD Detail
0.005 Metabolic syndrome X NA BeFree,GAD Detail
<0.001 Carotid Atherosclerosis NA BeFree Detail
<0.001 Carcinogenesis NA BeFree Detail
0.002 Choroidal Neovascularization NA GAD Detail
<0.001 Disorder of macula of retina NA BeFree Detail
0.003 Pregnancy associated hypertension NA LHGDN Detail
0.002 Ischemic stroke NA GAD Detail
0.002 Acute coronary syndrome NA GAD Detail
<0.001 Drusen NA BeFree Detail
0.002 Blood pressure finding NA GAD Detail
0.002 Systemic arterial pressure NA GAD Detail
0.005 Hypertriglyceridemia result NA GAD Detail
0.003 colorectal cancer NA BeFree,GAD Detail
0.002 Geographic Atrophy NA GAD Detail
<0.001 Peripheral Arterial Diseases NA BeFree Detail
0.001 Total Hypotrichosis, Mari type NA BeFree Detail
<0.001 Hypotrichosis simplex NA BeFree Detail
0.002 Venous thromboembolism NA GAD Detail
0.042 coronary artery disease NA BeFree,GAD,LHGDN Detail
0.240 High density lipoprotein cholesterol level quantitative trait locus 12 NA CLINVAR,CTD_human Detail
<0.001 Combined hyperlipidemia NA BeFree Detail
0.002 Infection of amniotic sac and membranes, unspecified, unspecified trimester, not applicable or unspecified NA GAD Detail
0.002 Cerebral Hemorrhage NA GAD Detail
0.001 Woolly Hair, Autosomal Recessive Expression studies of a novel splice site mutation in the LIPH gene identified i... BeFree 25271093 Detail
0.002 Alzheimer's disease NA GAD Detail
0.005 amyotrophic lateral sclerosis NA GAD Detail
<0.001 arteriosclerosis NA BeFree Detail
0.021 atherosclerosis NA BeFree,GAD,LHGDN Detail
0.002 Malignant neoplasm of urinary bladder NA GAD Detail
<0.001 Non-small cell lung carcinoma NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
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Lack of association between LIPC-514 C/T polymorphism of hepatic lipase and endometriosis in Iranian... DisGeNET Detail
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Variants -250G/A and -514C/T in the LIPC gene are associated with hypertensive disorders of pregnanc... DisGeNET Detail
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Ten non-synonymous single nucleotide polymorphisms (nsSNPs), which were recently associated with col... DisGeNET Detail
Ten non-synonymous single nucleotide polymorphisms (nsSNPs), which were recently associated with col... DisGeNET Detail
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Expression studies of a novel splice site mutation in the LIPH gene identified in a Japanese patient... DisGeNET Detail
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Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs386559608 dbSNP
Genome
hg19
Position
chr15:58,702,768-58,862,043
Variant Type
snv
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