CORIN, corin, serine peptidase, 10699

N. diseases: 55; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906894
rs387906894
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C3281288
Disease:
PREECLAMPSIA/ECLAMPSIA 5 		0.800 GeneticVariation UNIPROT Role of corin in trophoblast invasion and uterine spiral artery remodelling in pregnancy. 22437503 2012
dbSNP: rs387906895
rs387906895
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C3281288
Disease:
PREECLAMPSIA/ECLAMPSIA 5 		0.800 GeneticVariation UNIPROT Role of corin in trophoblast invasion and uterine spiral artery remodelling in pregnancy. 22437503 2012
dbSNP: rs387906894
rs387906894
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C3281288
Disease:
PREECLAMPSIA/ECLAMPSIA 5 		C 0.800 CausalMutation CLINVAR
dbSNP: rs387906895
rs387906895
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C3281288
Disease:
PREECLAMPSIA/ECLAMPSIA 5 		C 0.800 CausalMutation CLINVAR
dbSNP: rs16860432
rs16860432
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs16860432
rs16860432
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs16860535
rs16860535
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs16860535
rs16860535
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs4695266
rs4695266
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs4695266
rs4695266
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs4695266
rs4695266
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs111253292
rs111253292
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.030 GeneticVariation BEFREE A corin gene variant (T555I/Q568P) was identified in blacks with hypertension and cardiac hypertrophy. 22987923 2012
dbSNP: rs75770792
rs75770792
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.030 GeneticVariation BEFREE A corin gene variant (T555I/Q568P) was identified in blacks with hypertension and cardiac hypertrophy. 22987923 2012
dbSNP: rs111253292
rs111253292
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.030 GeneticVariation BEFREE The minor corin I555(P568) allele, defined by the T555I and Q568P mutations, is common in persons of African ancestry and associated with increased risk for hypertension and cardiac concentric hypertrophy. 19919978 2009
dbSNP: rs75770792
rs75770792
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.030 GeneticVariation BEFREE The minor corin I555(P568) allele, defined by the T555I and Q568P mutations, is common in persons of African ancestry and associated with increased risk for hypertension and cardiac concentric hypertrophy. 19919978 2009
dbSNP: rs111253292
rs111253292
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.030 GeneticVariation BEFREE We recently identified a minor allele in the corin gene defined by 2 highly linked single nucleotide polymorphisms (T555I and Q568P), which was associated with hypertension in blacks. 17296875 2007
dbSNP: rs75770792
rs75770792
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.030 GeneticVariation BEFREE We recently identified a minor allele in the corin gene defined by 2 highly linked single nucleotide polymorphisms (T555I and Q568P), which was associated with hypertension in blacks. 17296875 2007
dbSNP: rs2271037
rs2271037
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE The mutant-type T allele of rs2271037</span> and C allele of rs3749585 might increase the susceptibility to hypertension in this population. 29391274 2018
dbSNP: rs3749585
rs3749585
Entrez Id: 10699
Gene Symbol: CORIN
CORIN
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE The mutant-type T allele of rs2271037 and C allele of rs3749</span>585 might increase the susceptibility to hypertension in this population. 29391274 2018