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: rs10109984
rs10109984
0.925 0.080 8 47891114 intron variant T/C snv 0.54
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 < 0.001 1 2013 2013
dbSNP: rs1372047743
rs1372047743
8 47960120 missense variant C/T snv 9.7E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs7003908
rs7003908
0.716 0.320 8 47858141 intron variant C/A snv 0.66
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs7830743
rs7830743
8 47798394 missense variant A/G snv 0.12 0.13
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 < 0.001 1 2013 2013