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: rs10810657
rs10810657 		0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 2 2016 2019
dbSNP: rs10810657
rs10810657 		0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 2 2016 2019
dbSNP: rs10810657
rs10810657 		0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 2 2016 2019
dbSNP: rs10810657
rs10810657 		0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10810657
rs10810657 		0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.700 1.000 1 2018 2018
dbSNP: rs10810657
rs10810657 		0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin 		0.700 1.000 1 2016 2016
dbSNP: rs10810657
rs10810657 		0.827 0.080 9 16884588 regulatory region variant T/A;G snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 1.000 1 2019 2019