rs1801394, FASTKD3;MTRR

N. diseases: 101
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.
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.895 19 2000 2017
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.889 18 2000 2017
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.846 13 1999 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.100 0.900 10 2003 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.070 0.714 7 2008 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.070 0.714 7 2008 2016
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.060 0.667 6 2014 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.050 1.000 5 2003 2015
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2005 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 0.750 4 2002 2017
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
58 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2006 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2005 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2008 2017
Obesity
CUI: C0028754
Disease: Obesity
1111 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2007 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2008 2017
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2005 2019
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2013 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2003 2012
Hyperhomocysteinemia
CUI: C0598608
Disease: Hyperhomocysteinemia
45 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2014 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2015 2020
Malignant neoplasm of colon and/or rectum
502 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2002 2017
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.030 1.000 3 2003 2009
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2004 2014
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2009 2016
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2011 2018