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: rs1554606
rs1554606
0.925 0.120 7 22729088 intron variant T/A;G snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 < 0.001 1 2019 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.010 < 0.001 1 2012 2012
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.010 < 0.001 1 2013 2013
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases
0.010 < 0.001 1 2015 2015
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
0.010 < 0.001 1 2010 2010
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder
0.010 < 0.001 1 2019 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 < 0.001 1 2016 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.010 < 0.001 1 2018 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
0.010 < 0.001 1 2013 2013
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2019 2019
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0011206
Disease: Delirium
Delirium
0.010 < 0.001 1 2011 2011
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.010 < 0.001 1 2013 2013
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0028754
Disease: Obesity
Obesity
0.010 < 0.001 1 2019 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2019 2019
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2019 2019
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 < 0.001 1 2012 2012
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 < 0.001 1 2012 2012
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone
0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 < 0.001 1 2012 2012
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.020 0.500 2 2013 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.020 0.500 2 2015 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0028754
Disease: Obesity
Obesity
0.020 0.500 2 2017 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.020 0.500 2 2014 2019