Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs16917546
LOC105378327 ; ZNF365
0.851 0.040 10 62637778 intron variant T/C snv 0.29 6
rs7538876
PADI6
0.807 0.120 1 17395867 intron variant G/A snv 0.37 6
rs157935
LINC00513 ; LINC-PINT
0.851 0.040 7 130900794 intron variant T/G snv 0.28 4
rs214782
TGM3 ; LOC105372503
0.851 0.040 20 2301324 intron variant G/A snv 0.73 4
rs59586681 0.851 0.040 20 2239664 intron variant A/G;T snv 0.34 4
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv 4
rs12202284
LOC105374875
0.925 0.080 6 471136 intron variant C/A;T snv 3
rs2805831
PTCSC2
1.000 0.040 9 97704354 intron variant G/A snv 0.18 2
rs79824801
PAN2 ; IL23A
1.000 0.040 12 56334353 intron variant T/C snv 4.5E-02 2
rs142310826 1.000 0.040 4 178481702 intergenic variant T/A snv 1.7E-02 3
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1356844630
GLI1
0.925 0.160 12 57470802 stop gained C/T snv 4.0E-06 5
rs775248597
ATM
0.851 0.120 11 108229185 stop gained C/G;T snv 8.1E-06 5
rs786203714
PALB2
0.925 0.200 16 23635095 stop gained A/T snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151