Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs12263737
PLCE1-AS1 ; PLCE1
1.000 0.080 10 94285156 intron variant G/A snv 0.32 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs12438490
OCA2
15 28015163 intron variant C/T snv 7.3E-02 1
rs12508222
FAT4
0.925 0.080 4 125449492 missense variant G/A;T snv 4.3E-02; 2.0E-05 3
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs13042395
SLC52A3
0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 13
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs1323135
SDCBP2-AS1 ; FKBP1A ; FKBP1A-SDCBP2
20 1377208 non coding transcript exon variant G/C;T snv 1
rs1346291
LOC105375925
8 81339729 regulatory region variant A/G snv 0.78 1
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1364898025
ATM
0.925 0.080 11 108227656 missense variant G/A snv 3
rs1430055 2 16499521 intergenic variant G/A snv 0.61 2
rs145188037
IGFBP3
0.925 0.080 7 45914866 missense variant G/A snv 1.1E-02 9.9E-03 4
rs1453029 18 41000207 intergenic variant T/C snv 7.0E-02 1
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs151181
CLN3
1.000 0.040 16 28479196 intron variant T/C snv 0.32 2
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37