rs3184504, SH2B3;ATXN2

N. diseases: 92
Disease: Antiphospholipid Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Antiphospholipid Syndrome
CUI: C0085278
Disease: Antiphospholipid Syndrome
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