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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.100 0.867 15 2007 2020
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.100 0.867 15 2007 2020
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.100 0.833 12 2003 2014
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.100 0.818 11 2003 2014
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.090 0.667 9 1997 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.080 1.000 8 1999 2017
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
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.060 0.833 6 2006 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.060 0.667 6 2008 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.060 0.667 6 2008 2018
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 0.800 5 1998 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.050 0.600 5 1999 2013
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
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
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
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
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
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.333 3 2004 2017
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.333 3 2004 2017
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
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.333 3 2004 2017
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