rs6059655, RALY

N. diseases: 10
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.
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 2 2016 2019
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 2 2016 2019
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 2 2016 2019
Hair Color
CUI: C0018498
Disease: Hair Color
312 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2018 2018
melanoma
CUI: C0025202
Disease: melanoma
515 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2017 2017
Skin Pigmentation
CUI: C0037290
Disease: Skin Pigmentation
72 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2015 2015
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2016 2016
Suntan
CUI: C0406208
Disease: Suntan
94 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2018 2018
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.790 0.080 20 34077942 intron variant A/G snv 0.95 0.700 1.000 1 2016 2016