Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.010 < 0.001 1 2004 2004
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 < 0.001 1 2018 2018
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0025322
Disease: Premature Menopause
Premature Menopause
0.010 < 0.001 1 2016 2016
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 < 0.001 1 2014 2014
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
0.010 < 0.001 1 2016 2016
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 0.500 2 2011 2018
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.020 0.500 2 2007 2008
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 0.500 2 2011 2018
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.020 0.500 2 2011 2018
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
0.020 0.500 2 2008 2018
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0016412
Disease: Folic Acid Deficiency
Folic Acid Deficiency
0.020 0.500 2 2015 2015
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.020 0.500 2 2007 2019
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0021364
Disease: Male infertility
Male infertility
0.060 0.667 6 2014 2019
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.070 0.714 7 2008 2016
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.070 0.714 7 2008 2016
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 0.750 4 2002 2017
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
0.100 0.846 13 1999 2019
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome
0.100 0.889 18 2000 2017
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
0.100 0.895 19 2000 2017
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 0.900 10 2003 2018
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.050 1.000 5 2003 2015
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.040 1.000 4 2005 2019
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.040 1.000 4 2008 2017
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.040 1.000 4 2006 2017
dbSNP: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.040 1.000 4 2005 2019