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: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.840 0.500 4 2011 2019
dbSNP: rs12941356
rs12941356 		17 17813217 3 prime UTR variant A/G snv 0.46
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2016 2016
dbSNP: rs187408367
rs187408367 		1.000 0.080 17 17835546 intron variant G/A snv 3.8E-03
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4925115
rs4925115 		1.000 0.080 17 17818143 non coding transcript exon variant A/G snv 0.71
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2297508
rs2297508 		0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 2007 2008
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2008 2008
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.020 1.000 2 2013 2018
dbSNP: rs1889018
rs1889018 		0.925 0.080 17 17831426 intron variant G/A snv 0.45
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.020 1.000 2 2006 2008
dbSNP: rs1889018
rs1889018 		0.925 0.080 17 17831426 intron variant G/A snv 0.45
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2006 2008
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		Nutritional and Metabolic Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0026837
Disease: Muscle Rigidity
Muscle Rigidity 		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		0.010 1.000 1 2013 2013
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0040822
Disease: Tremor
Tremor 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11868035
rs11868035 		0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs13306741
rs13306741 		1.000 0.040 17 17811708 3 prime UTR variant C/A;T snv 4.3E-03; 7.4E-06
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1889018
rs1889018 		0.925 0.080 17 17831426 intron variant G/A snv 0.45
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2297508
rs2297508 		0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		Nutritional and Metabolic Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2297508
rs2297508 		0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2014 2014
dbSNP: rs2297508
rs2297508 		0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2007 2007