Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1209809979
AKR1A1
0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912576
SMAD4
1.000 0.120 18 51065539 stop gained G/T snv 1
rs121912577
SMAD4
0.925 0.160 18 51067115 stop gained C/G;T snv 8.0E-06 2
rs121912578
SMAD4
1.000 0.120 18 51078285 missense variant G/C snv 1
rs121912579
SMAD4
1.000 0.120 18 51078351 stop gained A/T snv 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121912661
TP53
1.000 0.120 17 7676264 missense variant C/A;G snv 1
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913527
KRAS
0.807 0.320 12 25225628 missense variant C/A;G;T snv 9
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1223231582
PRSS1
0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1235228469
PIK3CB
0.925 0.120 3 138684714 missense variant C/A snv 8.0E-06 2
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37 2
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs12456874
LDLRAD4
0.925 0.120 18 13366863 intron variant A/G snv 0.20 2
rs12478462 1.000 0.120 2 152798206 intergenic variant T/G snv 0.28 1
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs12620038
EPCAM-DT
1.000 0.120 2 47248996 intron variant C/G;T snv 1
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs1276300653
CAMK1 ; OGG1
0.925 0.120 3 9757072 missense variant T/C snv 7.0E-06 2