rs1805087, MTR

N. diseases: 135
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.
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1 2011 2011
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2001 2007
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2005 2005
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 0.800 5 2001 2012
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2014 2016
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2014 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2010 2010
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 1999 2004
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 1.000 3 2001 2005
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2001 2001
Attention deficit hyperactivity disorder
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
420 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2017 2018
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2000 2000
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2009 2016
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2014 2014
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2013 2013
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2007 2017
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2005 2007
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2011 2018
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2011 2011
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2018 2018
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2006 2008
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2004 2009