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: rs1056827
rs1056827
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs1056836
rs1056836
0.581 0.680 2 38071060 missense variant G/C snv 0.51
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2007 2007
dbSNP: rs162561
rs162561
2 38071734 intron variant T/G snv 0.85
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2018 2018