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: 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: 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: 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
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: 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: 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: 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: 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: 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: 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: 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: 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: rs73203093
rs73203093
RUNX1
1.000 0.040 21 35085209 intron variant C/G;T snv
CUI: C0013595
Disease: Eczema
Eczema 		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: rs9979383
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs9979383
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
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: 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: 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: 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: 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