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.
Encephalopathies
CUI: C0085584
Disease: Encephalopathies
64 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Neurodevelopmental Disorders
CUI: C1535926
Disease: Neurodevelopmental Disorders
14 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Obesity
CUI: C0028754
Disease: Obesity
1111 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2007 2007
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.040 0.750 4 2003 2008
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.667 3 2003 2008
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
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Cardiac Carcinoma
CUI: C1959584
Disease: Cardiac Carcinoma
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 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 pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 2008
obsolete Combined hyperlipidemia
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1.000 1 2008 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
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
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2004 2009
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2004 2009
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