Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 100128998
Gene Symbol: C20orf181
C20orf181
chromosome 20 open reading frame 181 0.479 0.885
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.070 None 1.000 7 0 1994 2019
Entrez Id: 260431
Gene Symbol: COPD
COPD
Pulmonary disease, chronic obstructive, severe early-onset 0.456 0.885
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.040 None 1.000 4 0 2019 2019
Entrez Id: 17
Gene Symbol: AAVS1
AAVS1
adeno-associated virus integration site 1 0.595 0.731
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.020 None 1.000 2 0 2005 2007
Entrez Id: 406906
Gene Symbol: MIR122
MIR122
microRNA 122 0.468 0.808
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.020 None 1.000 2 0 2014 2016
Entrez Id: 100187907
Gene Symbol: TRAP
TRAP
triiodothyronine receptor auxiliary protein 0.579 0.731
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 100505887
Gene Symbol: LINC01672
LINC01672
long intergenic non-protein coding RNA 1672 0.462 0.846
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 1989 1989
Entrez Id: 101180976
Gene Symbol: IFNL4
IFNL4
interferon lambda 4 (gene/pseudogene) 0.670 0.577
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 1 2017 2017
Entrez Id: 106480993
Gene Symbol: RN7SL263P
RN7SL263P
RNA, 7SL, cytoplasmic 263, pseudogene 0.496 0.808
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 117195
Gene Symbol: MRGPRX3
MRGPRX3
MAS related GPR family member X3 0.529 0.923
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 117196
Gene Symbol: MRGPRX4
MRGPRX4
MAS related GPR family member X4 0.531 0.923
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 145624
Gene Symbol: PWAR1
PWAR1
Prader Willi/Angelman region RNA 1 0.490 0.769
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2005 2005
Entrez Id: 259249
Gene Symbol: MRGPRX1
MRGPRX1
MAS related GPR family member X1 0.531 0.923
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 340451
Gene Symbol: CPP
CPP
ceruloplasmin pseudogene 0.631 0.731
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 3440
Gene Symbol: IFNA2
IFNA2
interferon alpha 2 0.442 0.885
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2002 2002
Entrez Id: 347745
Gene Symbol: PWAR4
PWAR4
Prader Willi/Angelman region RNA 4 0.573 0.769
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2002 2002
Entrez Id: 406899
Gene Symbol: MIR106A
MIR106A
microRNA 106a 0.524 0.846
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2016 2016
Entrez Id: 406974
Gene Symbol: MIR197
MIR197
microRNA 197 0.565 0.615
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2016 2016
Entrez Id: 440915
Gene Symbol: POTEKP
POTEKP
POTE ankyrin domain family member K, pseudogene 0.542 0.769
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 441931
Gene Symbol: VN1R17P
VN1R17P
vomeronasal 1 receptor 17 pseudogene 0.529 0.923
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 442206
Gene Symbol: GPR166P
GPR166P
G protein-coupled receptor 166 pseudogene 0.531 0.923
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 5175
Gene Symbol: PECAM1
PECAM1
platelet and endothelial cell adhesion molecule 1 0.426 0.846
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2019 2019
Entrez Id: 60498
Gene Symbol: IGAN1
IGAN1
IgA nephropathy 0.524 0.808
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 653108
Gene Symbol: CXADRP1
CXADRP1
CXADR pseudogene 1 0.463 0.846
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2019 2019
Entrez Id: 8205
Gene Symbol: TAM
TAM
Myeloproliferative syndrome, transient (transient abnormal 0.528 0.731
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 2008 2008
Entrez Id: 4018
Gene Symbol: LPA
LPA
lipoprotein(a) 0.444 0.769 6.6E-89
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
group 0.010 None 1.000 1 0 1995 1995