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.
Cancer of Digestive System
CUI: C0751075
Disease: Cancer of Digestive System
15 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1 2013 2013
Laryngeal cleft
CUI: C1840311
Disease: Laryngeal cleft
4 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1 2012 2012
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
Turner Syndrome
CUI: C0041408
Disease: Turner Syndrome
21 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.010 1 2015 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
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
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 0.500 2 2005 2013
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 0.500 2 2015 2015
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 0.500 2 1997 1999
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
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
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
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.030 0.667 3 2007 2018
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
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
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
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
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
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
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
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