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: rs12972366
rs12972366 		19 4920402 intron variant A/G snv 0.29
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1840221
rs1840221 		19 4932267 intron variant C/T snv 0.24
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2123731
rs2123731 		1.000 0.080 19 4929461 missense variant A/C;G snv 8.1E-06; 0.30
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2779165
rs2779165 		19 4915435 intron variant G/C;T snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs4807003
rs4807003 		19 4957122 intron variant G/A snv 0.24
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs2656927
rs2656927 		1.000 0.040 19 4908263 intron variant C/T snv 1.0E-01
CUI: C0028960
Disease: Oligospermia
Oligospermia 		Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs8103849
rs8103849 		1.000 0.040 19 4909617 missense variant C/G snv 0.38 0.40
CUI: C0028960
Disease: Oligospermia
Oligospermia 		Male Urogenital Diseases 0.010 1.000 1 2019 2019