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.
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2004 2004
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2014 2014
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2016 2016
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
90 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1 2018 2018
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
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2011 2018
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2008 2018
Folic Acid Deficiency
CUI: C0016412
Disease: Folic Acid Deficiency
8 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2015 2015
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2011 2018
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2007 2008
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 0.500 2 2007 2019
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
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
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
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
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
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
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
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
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