Source: GWASCAT

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: 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: 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: 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: rs2742552
rs2742552
11 8855305 intron variant C/T snv 0.51
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs34723331
rs34723331
11 8721319 intron variant C/- delins 0.33
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs35762459
rs35762459
11 8823106 intron variant -/A delins 0.46
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs3812762
rs3812762
1.000 0.120 11 8730093 missense variant G/C snv 0.32 0.27
CUI: C0848558
Disease: Hypospadias
Hypospadias
0.700 1.000 1 2014 2014
dbSNP: rs4579928
rs4579928
11 8794157 intron variant A/G snv 0.47
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs7120300
rs7120300
11 8801946 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs78406497
rs78406497
11 8804524 intron variant G/A snv 5.1E-02
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
0.700 1.000 1 2018 2018
dbSNP: rs7937298
rs7937298
11 8845962 intron variant G/C snv 0.33
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs7937298
rs7937298
11 8845962 intron variant G/C snv 0.33
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs7945705
rs7945705
11 8840983 intron variant G/A snv 0.32
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs871677
rs871677
11 8717296 intron variant T/C snv 0.34
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019