Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11887092
rs11887092
Entrez Id: 1281;105373791
Gene Symbol: COL3A1;LOC105373791
COL3A1;LOC105373791
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE The G allele of rs11887092 increased the risk of stroke recurrence in patients with atherothrombotic stroke (adjusted HR 1.59, 95 % CI 1.04-2.44, P = 0.035). 24664438 2014
dbSNP: rs1800255
rs1800255
Entrez Id: 1281
Gene Symbol: COL3A1
COL3A1
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE The A allele of rs1800255 in the COL3A1 gene coding region was significantly associated with a reduced risk of stroke recurrence in patients with lacunar infarction (adjusted hazard ratio [HR] 0.58, 95 % confidence interval [CI] 0.36-0.93, P = 0.024), but there was an increased risk of all-cause mortality of atherothrombotic patients (adjusted HR 1.43, 95 % CI 1.01-2.00, P = 0.044). 24664438 2014
dbSNP: rs2138533
rs2138533
Entrez Id: 1281;105373791
Gene Symbol: COL3A1;LOC105373791
COL3A1;LOC105373791
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE The TT genotype of rs2138533 showed a significantly increased risk of death caused by cardiovascular disease or stroke in lacunar infarct patients (adjusted HR 2.98, 95 % CI 1.27-6.98, P = 0.012), but there was a reduced risk of all-cause mortality for patients with intracerebral hemorrhage (adjusted HR 0.34, 95 % CI 0.12-0.93, P = 0.036). 24664438 2014