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: rs150498232
rs150498232
RUNX1 ; LOC100506403
21 35420326 intron variant A/G snv 2.3E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs16993221
rs16993221
RUNX1 ; LOC100506403
21 35477121 intron variant A/T snv 2.6E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.800 1.000 1 2013 2013
dbSNP: rs1883067
rs1883067
RUNX1
21 35027879 intron variant T/C snv 5.4E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs2242886
rs2242886
RUNX1
21 35015509 intron variant C/T snv 5.7E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2834655
rs2834655
RUNX1
21 34866210 intron variant G/A snv 0.28
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2834655
rs2834655
RUNX1
21 34866210 intron variant G/A snv 0.28
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs2834684
rs2834684
RUNX1
21 34940050 intron variant C/T snv 0.26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2834707
rs2834707
RUNX1
21 34971255 intron variant C/T snv 0.35
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs28567906
rs28567906
RUNX1
21 34911514 intron variant A/G snv 0.16
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs28567906
rs28567906
RUNX1
21 34911514 intron variant A/G snv 0.16
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs397774249
rs397774249
RUNX1
21 35293938 intron variant -/A;AA delins 0.38
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs56117721
rs56117721
RUNX1
21 35026289 intron variant T/A snv 5.3E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs56117721
rs56117721
RUNX1
21 35026289 intron variant T/A snv 5.3E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs73197346
rs73197346
RUNX1 ; LOC100506403
21 35397891 intron variant T/C snv 8.7E-02
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs73205303
rs73205303
RUNX1
21 35095533 intron variant G/A snv 9.8E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
dbSNP: rs73900579
rs73900579
RUNX1
21 34908600 intron variant T/C snv 0.15
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs73900579
rs73900579
RUNX1
21 34908600 intron variant T/C snv 0.15
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs75030518
rs75030518
RUNX1
21 34941487 intron variant G/A snv 1.7E-03
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs75030518
rs75030518
RUNX1
21 34941487 intron variant G/A snv 1.7E-03
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs75967349
rs75967349
RUNX1
21 35028144 intron variant C/G snv 3.2E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs8126516
rs8126516
RUNX1
21 35080321 intron variant G/A snv 0.13
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs8133974
rs8133974
RUNX1
21 35078544 intron variant C/T snv 0.11
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs8133974
rs8133974
RUNX1
21 35078544 intron variant C/T snv 0.11
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs8133974
rs8133974
RUNX1
21 35078544 intron variant C/T snv 0.11
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9976876
rs9976876
RUNX1
21 35598052 intron variant G/T snv 0.39
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018