Variant Gene Disease Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77375493
rs77375493
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia
0.030 GeneticVariation BEFREE Recent research has demonstrated in patients with MPN the existence of factors increasing the risk of SVT such as the presence of the JAK2 V617F mutation and its 46/1 haplotype. 23855810

2014

dbSNP: rs77375493
rs77375493
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia
0.030 GeneticVariation BEFREE In addition, our findings in JAK2(V617F)-negative SVT patients indicate an important role for the 46/1 haplotype in the etiology and diagnosis of SVT-related MPNs, independent of JAK2(V617F), that requires further exploration. 21364191

2011

dbSNP: rs77375493
rs77375493
CUI: C0039240
Disease: Supraventricular tachycardia
Supraventricular tachycardia
0.030 GeneticVariation BEFREE Anticoagulation therapy combined with low-dose aspirin and proper treatment of the MPD is recommended in patients with SVT associated with the JAK2(V617F) mutation. 17687555

2007