Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10743086
rs10743086
11 8753376 intron variant G/A snv 0.23
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs10743093
rs10743093
11 8847582 intron variant A/G snv 0.33
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10769960
rs10769960
11 8797456 intron variant T/C snv 0.34
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs10769966
rs10769966
11 8825494 intron variant C/A;T snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs10769967
rs10769967
11 8837183 intron variant G/C;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10769970
rs10769970
11 8896390 intron variant A/G snv 0.34
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10769971
rs10769971
11 8903729 intron variant C/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10769973
rs10769973
11 8907068 intron variant C/G snv 0.34
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10840133
rs10840133
11 8824822 intron variant G/A snv 0.44
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs10840134
rs10840134
11 8843816 intron variant T/C snv 0.32
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10840141
rs10840141
11 8880671 intron variant T/C snv 0.35
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10840142
rs10840142
11 8884531 intron variant A/G snv 0.34
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10840147
rs10840147
11 8899157 intron variant A/G snv 0.34
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10840148
rs10840148
11 8901981 intron variant C/T snv 0.34
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11042078
rs11042078
11 8805153 intron variant G/T snv 0.36
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11042103
rs11042103
11 8867153 intron variant C/T snv 0.33
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11603841
rs11603841
11 8813133 intron variant T/C snv 0.38
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1529641
rs1529641
11 8842591 intron variant T/G snv 0.40
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2568043
rs2568043
11 8842003 intron variant T/C snv 0.40
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2568061
rs2568061
11 8864713 intron variant A/G snv 0.55
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2568090
rs2568090
11 8827948 intron variant T/C snv 0.35
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2742540
rs2742540
11 8877981 intron variant A/G snv 0.41
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs2742540
rs2742540
11 8877981 intron variant A/G snv 0.41
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2742545
rs2742545
11 8862761 intron variant C/A;G snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2742552
rs2742552
11 8855305 intron variant C/T snv 0.51
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012