Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72653706
rs72653706
ABCC6
A 0.710 CausalMutation CLINVAR

dbSNP: rs121908029
rs121908029
LDLR
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913279
rs121913279
PIK3CA
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554810066
rs1554810066
ENG ; LOC105379841
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555517253
rs1555517253
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs1568362252
rs1568362252
NOTCH3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs199474657
rs199474657
ND1 ; ND2 ; TRNL1
G 0.700 CausalMutation CLINVAR

dbSNP: rs28933696
rs28933696
NOTCH3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs63749796
rs63749796
ABCC6
G 0.700 CausalMutation CLINVAR

dbSNP: rs63751241
rs63751241
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs72664204
rs72664204
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs72664207
rs72664207
ABCC6
C 0.700 CausalMutation CLINVAR

dbSNP: rs754360599
rs754360599
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs699
rs699
AGT
0.060 GeneticVariation BEFREE In this study we examined the relation of M235T polymorphism to cerebrovascular disease and carotid atheroma in 100 consecutive Caucasian patients with internal carotid artery territory ischaemia (TIA or stroke), presenting to a carotid ultrasound service. 8523390

1995
dbSNP: rs76863441
rs76863441
PLA2G7
0.020 GeneticVariation BEFREE A mutation in plasma platelet-activating factor acetylhydrolase (Val279-->Phe) is a genetic risk factor for stroke. 9412624

1997
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE The C677T MTHFR mutation was found in 19% of patients with stroke, 14% of patients with AVN, and 14% of patients with neither complication (P = NS). 9840906

1998
dbSNP: rs1255283120
rs1255283120
MTHFR
0.010 GeneticVariation BEFREE The C1565T GPIIIa mutation was found in 25% of patients with stroke, 14% of patients with AVN, and 18% of patients with neither complication (P = NS). 9840906

1998
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE Our data suggests that homozygosity for the MTHFR C677T polymorphism is a risk factor of RVO in addition to arterial hypertension and a family history of stroke. 9863710

1998
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control study. 9950259

1999
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE The odds ratio of stroke for C677T homozygotes, with other genotypes as a reference group, was 1.59, 95% CI=0.85, 2.97. 9974399

1999
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE According to our results, the C677T mutation does not constitute a major risk factor for transient ischemic attack or minor stroke, even under consideration of other possibly confounding factors that are known to affect plasma homocysteine levels. 10360632

1999
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE The odds ratio for stroke was not significantly increased in carriers of the prothrombin mutation (OR 1.2; 95% CI 0.1-10.7), FVL (OR 2.5; 95% CI 0.5-13.5), or the C677T mutation (OR 1.7; 95% CI 0.6-4.5). 10365738

1999
dbSNP: rs1188383936
rs1188383936
F2
0.050 GeneticVariation BEFREE The odds ratio for stroke was not significantly increased in carriers of the prothrombin mutation (OR 1.2; 95% CI 0.1-10.7), FVL (OR 2.5; 95% CI 0.5-13.5), or the C677T mutation (OR 1.7; 95% CI 0.6-4.5). 10365738

1999
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE The prevalence of the homozygous C677T mutation was not significantly higher in the elderly stroke patients (7%) than in the atherosclerotic risk (8%) or healthy elderly control (2%) groups. 10408794

1999
dbSNP: rs1217691063
rs1217691063
MTHFR
0.100 GeneticVariation BEFREE There was no difference in the proportion of patients with SCD with or without stroke who were homozygous for the C677T MTHFR mutation (0/11 versus 2/29; Fisher's, P = 1.000). 10524453

1999