Disease: Deep Vein Thrombosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918156
rs121918156
Entrez Id: 5624;105373608
Gene Symbol: PROC;LOC105373608
PROC;LOC105373608
CUI: C0149871
Disease:
Deep Vein Thrombosis 		T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
dbSNP: rs1321566264
rs1321566264
Entrez Id: 5624;105373608
Gene Symbol: PROC;LOC105373608
PROC;LOC105373608
CUI: C0149871
Disease:
Deep Vein Thrombosis 		T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
dbSNP: rs1553424043
rs1553424043
Entrez Id: 5624;100616187
Gene Symbol: PROC;MIR4783
PROC;MIR4783
CUI: C0149871
Disease:
Deep Vein Thrombosis 		C 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
dbSNP: rs369504169
rs369504169
Entrez Id: 5624
Gene Symbol: PROC
PROC
CUI: C0149871
Disease:
Deep Vein Thrombosis 		A 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
dbSNP: rs1799808
rs1799808
Entrez Id: 5624
Gene Symbol: PROC
PROC
CUI: C0149871
Disease:
Deep Vein Thrombosis 		0.010 GeneticVariation BEFREE Mutant alleles of rs1799808, rs6441600 and rs13062355 SNPs may contribute to DVT, whereas mutant alleles of rs1799810, rs6123 and rs12634349 may protect individuals from DVT. 31295762 2019
dbSNP: rs1799810
rs1799810
Entrez Id: 5624
Gene Symbol: PROC
PROC
CUI: C0149871
Disease:
Deep Vein Thrombosis 		0.010 GeneticVariation BEFREE Mutant alleles of rs1799808, rs6441600 and rs13062355 SNPs may contribute to DVT, whereas mutant alleles of rs1799810, rs6123 and rs12634349 may protect individuals from DVT. 31295762 2019
dbSNP: rs121918146
rs121918146
Entrez Id: 5624;105373608
Gene Symbol: PROC;LOC105373608
PROC;LOC105373608
CUI: C0149871
Disease:
Deep Vein Thrombosis 		0.010 GeneticVariation BEFREE Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosis. 30439769 2018
dbSNP: rs773761677
rs773761677
Entrez Id: 5624;105373608
Gene Symbol: PROC;LOC105373608
PROC;LOC105373608
CUI: C0149871
Disease:
Deep Vein Thrombosis 		0.010 GeneticVariation BEFREE The other mutations of Leu-34Pro and Thr295Ile with reduced PC activity and antigen levels were identified in Proband 2, a 19-year-old male with DVT. 25393254 2014