Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7593730
rs7593730
1.000 0.080 2 160314943 intron variant T/C snv 0.75
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.810 1.000 3 2010 2018
dbSNP: rs7572970
rs7572970
1.000 0.080 2 160280145 intron variant A/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 2 2010 2018
dbSNP: rs10178094
rs10178094
2 160479895 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs1020731
rs1020731
1.000 0.080 2 160287544 intron variant G/A snv 0.69
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs1020731
rs1020731
1.000 0.080 2 160287544 intron variant G/A snv 0.69
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs113678689
rs113678689
2 160450317 intron variant G/C;T snv
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs12692592
rs12692592
1.000 0.080 2 160306870 intron variant G/T snv 0.74
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs12692596
rs12692596
2 160409399 intron variant C/T snv 0.33
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs140902008
rs140902008
2 160380973 intron variant C/T snv 8.3E-03
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs148076191
rs148076191
2 160317974 intron variant G/A snv 1.1E-02
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs1563575
rs1563575
1.000 0.080 2 160275183 intron variant G/A snv 0.70
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4077463
rs4077463
1.000 0.080 2 160309723 intron variant A/G snv 0.74
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs4589705
rs4589705
1.000 0.080 2 160319625 intron variant T/A snv 0.75
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs6432622
rs6432622
2 160483759 intron variant A/G snv 0.50
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs7423572
rs7423572
2 160487551 intron variant C/G snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs7424771
rs7424771
2 160419867 intron variant G/A snv 0.44
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs7424771
rs7424771
2 160419867 intron variant G/A snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs7424771
rs7424771
2 160419867 intron variant G/A snv 0.44
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2019 2019
dbSNP: rs7424771
rs7424771
2 160419867 intron variant G/A snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs7425274
rs7425274
2 160346884 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1248131654
rs1248131654
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1248131654
rs1248131654
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1248131654
rs1248131654
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1248131654
rs1248131654
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
Neoplasms; Endocrine System Diseases 0.010 1.000 1 2013 2013