rs6136, SELP

N. diseases: 17
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.700 1.000 3 2018 2018
P-Selectin Measurement
CUI: C3890352
Disease: P-Selectin Measurement
2 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.700 1.000 1 2017 2017
Soluble P-Selectin Measurement
CUI: C4050627
Disease: Soluble P-Selectin Measurement
3 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.700 1.000 1 2010 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.030 1.000 3 2001 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.030 0.667 3 2001 2007
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.020 1.000 2 2007 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.020 1.000 2 2001 2006
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.020 0.500 2 2006 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.020 1.000 2 2002 2014
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.020 1.000 2 2007 2008
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
CUI: C1832661
Disease: ANOPHTHALMIA AND PULMONARY HYPOPLASIA
80 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.010 1.000 1 2014 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.010 1.000 1 2006 2006
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.010 1.000 1 2006 2006
Cachexia
CUI: C0006625
Disease: Cachexia
11 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.010 1.000 1 2014 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.010 1.000 1 2007 2007
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.010 1.000 1 2007 2007
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.010 1.000 1 2014 2014