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: 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: 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: 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: rs11088309
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 2 2019 2019
dbSNP: rs68088846
rs68088846
RUNX1 ; LOC102724584
0.807 0.080 21 34835870 intron variant G/A snv 0.27
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		0.700 1.000 2 2016 2017
dbSNP: rs68088846
rs68088846
RUNX1 ; LOC102724584
0.807 0.080 21 34835870 intron variant G/A snv 0.27
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		0.700 1.000 2 2016 2017
dbSNP: rs68088846
rs68088846
RUNX1 ; LOC102724584
0.807 0.080 21 34835870 intron variant G/A snv 0.27
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		0.700 1.000 2 2016 2017
dbSNP: rs68088846
rs68088846
RUNX1 ; LOC102724584
0.807 0.080 21 34835870 intron variant G/A snv 0.27
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 2 2016 2017
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: rs68088846
rs68088846
RUNX1 ; LOC102724584
0.807 0.080 21 34835870 intron variant G/A snv 0.27
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		0.700 1.000 2 2016 2017
dbSNP: rs9979383
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs11088309
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs11701104
rs11701104
RUNX1
1.000 0.080 21 34866220 intron variant C/T snv 0.18
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
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: 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: 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: rs2014300
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 1.000 1 2011 2011
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: rs2834787
rs2834787
RUNX1
1.000 0.080 21 35130261 intron variant A/G snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
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