Source: CURATED ×
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: rs2084898
rs2084898
TRIM29
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke. 22990015

2012
dbSNP: rs7506045
rs7506045
IMPA2
0.800 GeneticVariation GWASDB A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. 17434096

2007
dbSNP: rs7506045
rs7506045
IMPA2
0.800 GeneticVariation GWASCAT A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. 17434096

2007
dbSNP: rs2230500
rs2230500
PRKCH
0.720 GeneticVariation GWASDB A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. 17206144

2007
dbSNP: rs2304556
rs2304556
FMNL2
0.700 GeneticVariation GWASDB Although no single SNP reached genome-wide significance (P < 5 × 10(-8)), we identified two SNPs in chromosome 2q23.3, rs2304556 (in FMNL2; P = 1.2 × 10(-7)) and rs1986743 (in ARL6IP6; P = 2.7 × 10(-7)), strongly associated with early-onset stroke. 22384361

2011
dbSNP: rs1986743
rs1986743
ARL6IP6
0.700 GeneticVariation GWASDB Although no single SNP reached genome-wide significance (P < 5 × 10(-8)), we identified two SNPs in chromosome 2q23.3, rs2304556 (in FMNL2; P = 1.2 × 10(-7)) and rs1986743 (in ARL6IP6; P = 2.7 × 10(-7)), strongly associated with early-onset stroke. 22384361

2011
dbSNP: rs556621
rs556621 		A 0.820 GeneticVariation GWASCAT Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. 22941190

2012
dbSNP: rs556621
rs556621 		A 0.820 GeneticVariation GWASDB Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. 22941190

2012
dbSNP: rs10890917
rs10890917 		0.700 GeneticVariation GWASDB Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. 22941190

2012
dbSNP: rs1767788
rs1767788 		0.700 GeneticVariation GWASDB Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. 22941190

2012
dbSNP: rs4711790
rs4711790 		0.700 GeneticVariation GWASDB Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. 22941190

2012
dbSNP: rs4714801
rs4714801 		0.700 GeneticVariation GWASDB Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. 22941190

2012