rs12203592, IRF4

N. diseases: 38
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hair Color
CUI: C0018498
Disease: Hair Color
312 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.800 1.000 3 2008 2013
Eye Color
CUI: C0015396
Disease: Eye Color
31 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.800 1.000 2 2010 2018
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.800 1.000 1 2011 2011
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.710 1.000 3 2011 2019
Skin Pigmentation
CUI: C0037290
Disease: Skin Pigmentation
72 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 3 2013 2018
Suntan
CUI: C0406208
Disease: Suntan
94 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 3 2013 2018
Alopecia, Androgenetic, 1
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
104 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2017
Alopecia, Androgenetic, 2
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
104 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2017
Alopecia, Androgenetic, 3
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
104 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2017
Alopecia, Male Pattern
CUI: C4083212
Disease: Alopecia, Male Pattern
743 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2017
Androgenetic Alopecia
CUI: C0162311
Disease: Androgenetic Alopecia
107 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2017
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2019
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2019
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2019
Melanosis
CUI: C0025209
Disease: Melanosis
23 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2010 2018
Other alopecia
CUI: C0029489
Disease: Other alopecia
104 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 2 2016 2017
Alopecia
CUI: C0002170
Disease: Alopecia
375 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 1 2017 2017
Freckles
CUI: C0016689
Disease: Freckles
10 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 1 2010 2010
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 1 2013 2013
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 1 2016 2016
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 1.000 1 2019 2019
Skin-Hair-Eye Pigmentation, Variation In, 8
CUI: C2673265
Disease: Skin-Hair-Eye Pigmentation, Variation In, 8
1 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.700 0
melanoma
CUI: C0025202
Disease: melanoma
515 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.060 1.000 6 2010 2017
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.649 0.320 6 396321 intron variant C/T snv 0.10 0.030 1.000 3 2011 2019