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: rs16891982
rs16891982
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs35407
rs35407
0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
Neoplasms 0.700 1.000 1 2016 2016