Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4866
NUDT1
0.827 0.240 7 2249951 missense variant G/A snv 2.2E-02 1.8E-02 5
rs1778335
PIP4K2A
1.000 0.080 10 22643219 intron variant T/C snv 0.27 1
rs7519667
WDR64
1.000 0.080 1 241722005 intron variant C/T snv 0.78 1
rs750078923
MYO18B
1.000 0.080 22 25769052 missense variant G/A;C snv 1.6E-05 1
rs1429133479
MYO18B
1.000 0.080 22 25847461 missense variant G/A snv 1.4E-05 1
rs12200782
BTN3A1
1.000 0.080 6 26402808 intron variant C/G snv 7.9E-02 1
rs141670911 1.000 0.080 6 26581030 intergenic variant A/T snv 7.3E-02 1
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs114033761 1.000 0.080 6 31093784 regulatory region variant T/C snv 1
rs116427960
HLA-B
0.925 0.120 6 31351449 intron variant C/G;T snv 3
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs141877527 1.000 0.080 10 33497992 intergenic variant A/G snv 7.3E-03 1
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 8
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs587776783
LOC112268118 ; RB1
0.851 0.200 13 48373493 splice donor variant G/A snv 5