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: 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: 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: 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: rs68088846
rs68088846
RUNX1 ; LOC102724584
0.807 0.080 21 34835870 intron variant G/A snv 0.27
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
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: 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: 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: 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: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		0.700 1.000 2 2016 2017
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: 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: 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: 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: 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: 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: 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: 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: 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
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: 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: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 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: 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: 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: 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