Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000668
TMC1
9 72790943 intron variant T/A;G snv 1
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs10058728
CSNK1A1
1.000 0.080 5 149524529 intron variant A/T snv 0.64 2
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1014867
FAT4
0.925 0.080 4 125491736 missense variant C/T snv 4.9E-02 4.9E-02 3
rs10186527
FLACC1
2 201335852 intron variant C/T snv 0.54 1
rs10191793
ST6GAL2
2 106809420 intron variant A/G snv 0.21 1
rs10197246
FLACC1
2 201340018 intron variant T/C snv 0.72 1
rs10201587
FLACC1
2 201338068 intron variant A/G snv 0.47 1
rs10274928
JAZF1
7 28102469 intron variant A/G;T snv 2
rs1035142
FLACC1
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs1039808
FAT4
0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 3
rs1042026
ADH1B
1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10454127
FLACC1
2 201347651 intron variant G/A;T snv 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10502995 18 55138645 regulatory region variant G/A snv 0.20 1
rs1050631
SLC39A6
0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30 4
rs10509670
PLCE1
0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56