rs79154414
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
|
28424481 |
2017 |
rs4581
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Val247Leu β2-glycoprotein-I allelic variant is associated with antiphospholipid syndrome: systematic review and meta-analysis.
|
22246055 |
2012 |
rs10774625
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Within this region, a TAC risk haplotype comprising one SNP in SH2B3 gene (rs3184504) and two SNPs in ATXN2 gene (rs10774625 and rs653178) exhibited the strongest association with thrombotic antiphospholipid syndrome (p-value = 5,9 × 10(-4) OR 95% CI 1.84 (1.32-2.55)).
|
23844121 |
2013 |
rs653178
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Within this region, a TAC risk haplotype comprising one SNP in SH2B3 gene (rs3184504) and two SNPs in ATXN2 gene (rs10774625 and rs653178) exhibited the strongest association with thrombotic antiphospholipid syndrome (p-value = 5,9 × 10(-4) OR 95% CI 1.84 (1.32-2.55)).
|
23844121 |
2013 |
rs3184504
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Within this region, a TAC risk haplotype comprising one SNP in SH2B3 gene (rs3184504) and two SNPs in ATXN2 gene (rs10774625 and rs653178) exhibited the strongest association with thrombotic antiphospholipid syndrome (p-value = 5,9 × 10(-4) OR 95% CI 1.84 (1.32-2.55)).
|
23844121 |
2013 |
rs899127658
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We examined the prevalence of prothrombotic polymorphisms (G1691A of factor V gene [FV Leiden] and G20210A of prothrombin [FII] gene), deficiencies of natural anticoagulants (protein C, protein S and antithrombin III) and antiphospholipid syndrome (APS) in patients with early ST-segment elevation MI (STEMI).
|
28647870 |
2017 |
rs6025
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Two young siblings who presented with an unusual recurrent severe thromboembolic phenomenon were found to have familial anti-phospholipid syndrome and were heterozygous for the factor V R506Q mutation.
|
8757529 |
1996 |
rs12570849
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
|
28424481 |
2017 |
rs1020096
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
|
28424481 |
2017 |
rs1217691063
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Hyperhomocyteinemia and the C677T/MTHFR mutation are not common in women with antiphospholipid syndrome.
|
15284001 |
2004 |
rs121918027
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Combined Ala601-Thr-type dysplasminogenaemia and antiphospholipid antibody syndrome in a patient with recurrent thrombosis.
|
12091052 |
2002 |
rs662
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association between paraoxonase-1 gene Q192R and L55M polymorphisms in systemic lupus erythematosus (SLE) and anti-phospholipid syndrome (APS) in a population from Cairo of Egypt.
|
28185016 |
2017 |
rs854560
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association between paraoxonase-1 gene Q192R and L55M polymorphisms in systemic lupus erythematosus (SLE) and anti-phospholipid syndrome (APS) in a population from Cairo of Egypt.
|
28185016 |
2017 |
rs1024843
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
|
28424481 |
2017 |
rs6104
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Genotype Ser413/Ser of PAI-2 polymorphism Ser413/Cys is associated with anti-phospholipid syndrome and systemic lupus erythematosus in a familial case: comparison with healthy controls.
|
17657675 |
2007 |
rs2788869
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
|
28424481 |
2017 |
rs2288493
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
|
28424481 |
2017 |