Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913355
rs121913355
17 0.699 0.393 7 140781602 stop lost C/A,G,T snp 4.0E-06 0.810 1.000 3 2002 2007
dbSNP: rs121913357
rs121913357
11 0.744 0.286 7 140781603 stop gained C/A,G,T snp 0.810 1.000 2 2004 2004
dbSNP: rs121913338
rs121913338
17 0.707 0.321 7 140753354 missense variant T/A,C,G snp 0.810 1.000 1 2004 2004
dbSNP: rs114216685
rs114216685
1 1.000 0.107 8 94391640 missense variant T/C snp 8.8E-04 8.3E-04 0.800 1 1999 1999
dbSNP: rs121908689
rs121908689
1 1.000 0.107 1 46272758 missense variant T/A snp 0.800 1 1999 1999
dbSNP: rs28936699
rs28936699
1 1.000 0.107 2 201209388 missense variant C/T snp 0.800 1 2002 2002
dbSNP: rs104894176
rs104894176
2 0.923 0.107 10 70598599 stop gained C/T snp 1.6E-05 0.700 4 1999 2006
dbSNP: rs121909775
rs121909775
2 1.000 0.107 2 201205929 stop gained C/A,T snp 4.0E-06 0.700 2 2002 2002
dbSNP: rs1023835002
rs1023835002
10 0.756 0.250 15 44711547 start lost A/G snp 0.700 1 2016 2016
dbSNP: rs1057519877
rs1057519877
10 0.756 0.250 15 44711549 start lost G/A snp 0.700 1 2016 2016
dbSNP: rs1057519879
rs1057519879
10 0.756 0.250 15 44711548 start lost T/C,G snp 0.700 1 2016 2016
dbSNP: rs1057519894
rs1057519894
2 0.923 0.143 7 148811650 missense variant T/A,G snp 0.700 1 2016 2016
dbSNP: rs1057519909
rs1057519909
6 0.801 0.250 15 66435116 missense variant A/C snp 0.700 1 2016 2016
dbSNP: rs1057519918
rs1057519918
MYC
5 0.846 0.214 8 127738390 missense variant C/T snp 0.700 1 2016 2016
dbSNP: rs1057519941
rs1057519941
7 0.821 0.179 3 179203761 missense variant T/C,G snp 0.700 1 2016 2016
dbSNP: rs1057519942
rs1057519942
8 0.801 0.214 3 179203760 missense variant G/A snp 0.700 1 2016 2016
dbSNP: rs1057519952
rs1057519952
5 0.878 0.143 3 49375577 missense variant G/A snp 0.700 1 2016 2016
dbSNP: rs1057519953
rs1057519953
5 0.878 0.143 3 49375576 missense variant C/A,T snp 0.700 1 2016 2016
dbSNP: rs1057519954
rs1057519954
3 0.878 0.143 3 49375465 missense variant T/A,C,G snp 0.700 1 2016 2016
dbSNP: rs1057520002
rs1057520002
19 0.692 0.357 17 7674242 missense variant A/C,G snp 0.700 1 2016 2016
dbSNP: rs1057520007
rs1057520007
19 0.699 0.321 17 7674917 missense variant T/A,C,G snp 0.700 1 2016 2016
dbSNP: rs1057520008
rs1057520008
17 0.707 0.393 17 7674918 stop lost A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs121434595
rs121434595
19 0.692 0.357 1 114716124 missense variant C/A,G,T snp 0.700 1 2016 2016
dbSNP: rs121434596
rs121434596
18 0.707 0.357 1 114716123 missense variant C/A,G,T snp 4.0E-06; 4.0E-06 0.700 1 2016 2016
dbSNP: rs267601394
rs267601394
5 0.878 0.179 7 148811635 missense variant T/A,G snp 0.700 1 2016 2016