rs344781, PLAUR

N. diseases: 7
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.
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 0.010 1.000 1 2008 2008
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 0.010 1.000 1 2014 2014
Headache
CUI: C0018681
Disease: Headache
75 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 0.010 1.000 1 2014 2014
Idiopathic pulmonary arterial hypertension
CUI: C3203102
Disease: Idiopathic pulmonary arterial hypertension
24 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 0.010 1.000 1 2011 2011
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 0.010 1.000 1 2011 2011
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 0.010 1.000 1 2016 2016
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 0.010 1.000 1 2011 2011