rs11066301, PTPN11

N. diseases: 12
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.
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2016 2016
Myositis
CUI: C0027121
Disease: Myositis
43 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2009 2009
Platelet mean volume determination (procedure)
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
371 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2009 2009
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.700 1.000 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.200 12 112433568 intron variant A/G snv 0.30 0.010 1.000 1 2014 2014