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: 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: 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: rs8129030
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs2014300
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.720 1.000 1 2012 2019
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: 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: rs8129030
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		0.700 1.000 1 2013 2013
dbSNP: rs9979383
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 3 2012 2016
dbSNP: rs8133843
rs8133843
RUNX1
1.000 0.120 21 35365944 intron variant G/A snv 0.65
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2014 2019
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: rs9979383
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		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: 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: 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: 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: rs8128234
rs8128234
RUNX1
1.000 0.040 21 35098568 intron variant C/T snv 0.26
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs8129030
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72
CUI: C3890205
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		0.700 1.000 1 2013 2013
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: rs68088846
rs68088846
RUNX1 ; LOC102724584
0.807 0.080 21 34835870 intron variant G/A snv 0.27
CUI: C0029489
Disease: Other alopecia
Other alopecia 		0.700 1.000 2 2016 2017
dbSNP: rs8129030
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72
CUI: C3898105
Disease: Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs8129030
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease 		0.700 1.000 1 2013 2013
dbSNP: rs8129030
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs117440128
rs117440128
RUNX1
1.000 0.080 21 35801864 intron variant G/A snv 6.2E-03
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		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: 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