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: rs1000113
rs1000113
0.925 0.040 5 150860514 intron variant C/T snv 0.13
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 1.000 1 2009 2009
dbSNP: rs10001410
rs10001410
1.000 0.040 4 61608511 intron variant C/A snv 0.55
Attention deficit hyperactivity disorder
0.010 1.000 1 2019 2019
dbSNP: rs1000256867
rs1000256867
17 7673550 missense variant T/A;G snv 4.0E-06
High-Grade Squamous Intraepithelial Lesions
0.010 1.000 1 2020 2020
dbSNP: rs1000283
rs1000283
0.925 0.080 1 209721316 intron variant G/A snv 0.18
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2011 2011
dbSNP: rs1000283
rs1000283
0.925 0.080 1 209721316 intron variant G/A snv 0.18
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2011 2011
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2011 2011
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD)
0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2015 2015
dbSNP: rs10004195
rs10004195
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
0.010 1.000 1 2019 2019
dbSNP: rs1000592
rs1000592
1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder
0.010 1.000 1 2014 2014
dbSNP: rs1000731
rs1000731
1.000 0.040 1 231827745 intron variant C/T snv 0.23
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 < 0.001 1 2018 2018
dbSNP: rs1000778
rs1000778
1.000 0.040 11 61887833 intron variant A/G snv 0.59
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2017 2017
dbSNP: rs10008257
rs10008257
0.925 0.040 4 94435177 intergenic variant G/A snv 0.63
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2008 2008
dbSNP: rs10008492
rs10008492
1.000 0.120 4 38764099 intergenic variant C/G;T snv
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin
0.010 1.000 1 2009 2009
dbSNP: rs10009145
rs10009145
1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.010 1.000 1 2012 2012
dbSNP: rs10009228
rs10009228
4 40354405 missense variant A/G snv 0.78 0.76
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs1000952
rs1000952
1.000 0.040 3 184038034 missense variant G/A;C;T snv 0.66; 3.6E-05; 4.0E-06
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder
0.010 1.000 1 2014 2014
dbSNP: rs10010131
rs10010131
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2008 2008
dbSNP: rs10010131
rs10010131
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.010 1.000 1 2009 2009