Source: BEFREE

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: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 1.000 1 2019 2019
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2012 2012
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0014742
Disease: Erythema Multiforme
Erythema Multiforme
0.010 1.000 1 2017 2017
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease
0.010 1.000 1 2009 2009
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2016 2016
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.010 1.000 1 2014 2014
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 1.000 1 2016 2016
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0042076
Disease: Urologic Neoplasms
Urologic Neoplasms
0.010 < 0.001 1 2018 2018
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.010 1.000 1 2012 2012
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 1.000 1 2018 2018
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2016 2016
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.010 1.000 1 2009 2009
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.010 1.000 1 2017 2017
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.010 1.000 1 2007 2007
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.010 1.000 1 2015 2015
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C1378703
Disease: Renal carcinoma
Renal carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2016 2016
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2015 2015
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0848548
Disease: hypertensive nephropathy
hypertensive nephropathy
0.010 1.000 1 2011 2011
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer
0.010 1.000 1 2018 2018
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2010 2010
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs699947
rs699947
0.570 0.680 6 43768652 upstream gene variant A/C;T snv
Exudative age-related macular degeneration
0.010 1.000 1 2016 2016