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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.080 1.000 8 2001 2019
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 1.000 5 2010 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 1.000 5 2010 2018
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.040 1.000 4 2002 2012
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.040 1.000 4 2012 2019
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.040 1.000 4 2003 2015
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
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 1.000 3 2002 2017
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2012 2012
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
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
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
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2005 2011
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
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
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 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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2005 2011
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
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
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2003 2010
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2007 2011
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2005 2011
Retinoblastoma
CUI: C0035335
Disease: Retinoblastoma
193 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2010 2015