Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1034749666
OLIG2
0.776 0.160 21 33027257 missense variant G/A snv 9
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs1214285376
XRCC1
0.776 0.200 19 43543490 missense variant G/T snv 4.0E-06 8
rs104894104
CDKN2A
0.790 0.160 9 21971019 missense variant G/A;T snv 7
rs148611340
XRCC1
0.790 0.120 19 43543621 missense variant G/A;C snv 4.0E-06; 1.2E-05 7
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs753152604
CDK4
0.827 0.040 12 57751680 missense variant C/A snv 7
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs1537375
CDKN2B-AS1
0.882 0.120 9 22116072 intron variant T/C;G snv 6
rs1642785
TP53
0.807 0.200 17 7676483 5 prime UTR variant G/A;C;T snv 1.2E-05; 0.67; 2.8E-05 6
rs5744533
POLK ; CERT1
0.807 0.120 5 75510279 intron variant C/A;T snv 6
rs1385943435
PAX5 ; LOC105376032
0.851 0.040 9 37002662 missense variant C/A;G;T snv 4.1E-06; 4.1E-06 5
rs374052197
PDPN
0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs760031382
PAX5
0.851 0.040 9 36966613 missense variant C/T snv 8.0E-06 5
rs769790595
IL4R
0.827 0.120 16 27360785 missense variant G/A;C snv 2.0E-05; 4.0E-06 5
rs865880036
MEIS2
0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs648044
ZBTB16 ; LOC101928875
0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 4
rs6489769
RAD52
0.851 0.120 12 963799 intron variant C/A;T snv 4
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4