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: rs34440547
rs34440547 		19 15472052 missense variant C/A;G;T snv 3.7E-05; 1.2E-05; 0.22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs36020076
rs36020076 		19 15469479 synonymous variant G/A;T snv 0.22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3813135
rs3813135 		19 15476534 missense variant T/C snv 0.36 0.37
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4638719
rs4638719 		19 15472751 intron variant A/G snv 0.38
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs60292400
rs60292400 		19 15471569 intron variant C/T snv 2.0E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8105422
rs8105422 		19 15475078 intron variant A/G snv 0.38
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs892145
rs892145 		1.000 0.040 19 15475861 missense variant A/T snv 0.36 0.38
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs733731
rs733731 		1.000 0.040 19 15476374 missense variant C/G;T snv 0.36
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs892145
rs892145 		1.000 0.040 19 15475861 missense variant A/T snv 0.36 0.38
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2014 2014