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: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0018498
Disease: Hair Color
Hair Color
0.800 1.000 3 2008 2013
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0015396
Disease: Eye Color
Eye Color
0.800 1.000 2 2010 2018
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.800 1.000 1 2011 2011
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.710 1.000 2 2011 2019
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
0.700 1.000 3 2013 2018
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0406208
Disease: Suntan
Suntan
0.700 1.000 3 2013 2018
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
0.700 1.000 2 2016 2019
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm
0.700 1.000 2 2016 2019
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3
0.700 1.000 2 2016 2017
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia
0.700 1.000 2 2016 2017
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1
0.700 1.000 2 2016 2017
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
0.700 1.000 2 2016 2019
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern
0.700 1.000 2 2016 2017
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0025209
Disease: Melanosis
Melanosis
0.700 1.000 2 2010 2018
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2
0.700 1.000 2 2016 2017
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0029489
Disease: Other alopecia
Other alopecia
0.700 1.000 2 2016 2017
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2016 2016
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0002170
Disease: Alopecia
Alopecia
0.700 1.000 1 2017 2017
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
0.700 1.000 1 2016 2016
dbSNP: rs12203592
rs12203592
0.649 0.320 6 396321 intron variant C/T snv 0.10
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019