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: rs823156
rs823156 		1.000 0.040 1 205795512 non coding transcript exon variant G/A snv 0.77 0.70
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.850 1.000 7 2011 2019
dbSNP: rs708730
rs708730 		1.000 0.040 1 205808652 intron variant G/A snv 0.66
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.720 1.000 4 2011 2015
dbSNP: rs1775148
rs1775148 		1.000 0.080 1 205788696 downstream gene variant C/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2014 2014
dbSNP: rs708727
rs708727 		1 205798757 synonymous variant G/A snv 0.30 0.29
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs708727
rs708727 		1 205798757 synonymous variant G/A snv 0.30 0.29
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs11240569
rs11240569 		1.000 0.040 1 205810103 synonymous variant G/A snv 0.29 0.23
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2015 2016
dbSNP: rs1305279636
rs1305279636 		1.000 0.040 1 205796947 missense variant G/A snv 1.2E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2010 2013
dbSNP: rs373421823
rs373421823 		1.000 0.040 1 205798782 missense variant C/T snv 3.2E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs823154
rs823154 		1.000 0.080 1 205793278 intron variant C/T snv 0.32
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 2015 2015