Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs57142672
rs57142672 		0.882 0.040 1 17418040 intron variant A/C;G;T snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs57142672
rs57142672 		0.882 0.040 1 17418040 intron variant A/C;G;T snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs57142672
rs57142672 		0.882 0.040 1 17418040 intron variant A/C;G;T snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs7528427
rs7528427 		0.882 0.040 1 17419777 intron variant C/T snv 0.36
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs7528427
rs7528427 		0.882 0.040 1 17419777 intron variant C/T snv 0.36
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs7528427
rs7528427 		0.882 0.040 1 17419777 intron variant C/T snv 0.36
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		Neoplasms 0.700 1.000 1 2019 2019