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: rs12601930
rs12601930 		1.000 0.040 17 39633179 non coding transcript exon variant C/T snv 1.6E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1495099
rs1495099 		17 39628211 intron variant C/G snv 0.54
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2271309
rs2271309 		17 39628737 intron variant G/A;T snv 0.60
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs907094
rs907094 		1.000 0.040 17 39634118 intron variant G/A snv 0.69 0.60
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs907094
rs907094 		1.000 0.040 17 39634118 intron variant G/A snv 0.69 0.60
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 0.500 2 2008 2008
dbSNP: rs12601930
rs12601930 		1.000 0.040 17 39633179 non coding transcript exon variant C/T snv 1.6E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 < 0.001 1 2008 2008
dbSNP: rs3764352
rs3764352 		1.000 0.040 17 39634686 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 < 0.001 1 2008 2008