rs10810657, None

N. diseases: 7
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 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 2 2016 2019
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 2 2016 2019
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 2 2016 2019
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 1 2019 2019
Skin Pigmentation
CUI: C0037290
Disease: Skin Pigmentation
72 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 1 2018 2018
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 1 2019 2019
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 1 2016 2016