Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs3212948
ERCC1
0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs4024
AFP
0.827 0.120 4 73435667 intron variant G/A snv 0.52 7
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs738791
MMP11
0.851 0.120 22 23775338 intron variant C/T snv 0.37 6
rs2289937
RAD21
0.882 0.080 8 116861572 intron variant G/A;C snv 4
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs3917412
C1orf112 ; SELE
1.000 0.040 1 169731361 intron variant T/A;C;G snv 4
rs4579555
RAD21
0.882 0.080 8 116867092 intron variant A/G snv 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs4328905
HPSE
4 83322396 intron variant A/G snv 0.18 0.18 1
rs6737848
SOCS5 ; LINC01118
2 46701027 intron variant C/G snv 0.14 1
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1114167628
PTEN
0.925 0.080 10 87961033 stop gained -/ATATCTAG delins 5
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490