Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200476704
TRAPPC1 ; CNTROB ; KCNAB3
1.000 0.040 17 7930659 stop gained G/A;C snv 2.4E-05 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 1
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 2
rs137853080
STK11
1.000 0.040 19 1207058 missense variant T/G snv 1
rs137853081
STK11
1.000 0.040 19 1219352 missense variant G/C;T snv 1
rs121909234
PTEN
1.000 0.040 10 87957867 missense variant G/A snv 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 3
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 2
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 2
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 1
rs587782228
MUTYH
0.882 0.120 1 45330557 missense variant C/A;T snv 4.2E-06; 4.2E-06 1
rs149617956
MITF
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 1
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 1