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: rs12050260
rs12050260 		14 23291885 intron variant T/C snv 0.56
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2017 2019
dbSNP: rs1057119
rs1057119 		14 23277060 synonymous variant C/G;T snv 0.21; 2.8E-05
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2295124
rs2295124 		14 23286389 intron variant A/G snv 0.75
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1055061
rs1055061 		1.000 0.040 14 23275723 missense variant C/T snv 7.0E-02; 4.1E-06 9.5E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2010 2010