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: rs13014235
rs13014235
0.851 0.040 2 201350769 missense variant C/G snv 0.62 0.63
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs2080303
rs2080303
0.882 0.040 2 201300483 intron variant T/C snv 0.72
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs6714430
rs6714430
0.882 0.040 2 201288961 intron variant C/T snv 0.72
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
Neoplasms 0.700 1.000 1 2019 2019