Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs773862672
MTOR
0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs149627368
REL
2 60922344 missense variant T/C snv 1.5E-04 1.0E-04 1
rs2227945
BRCA1
1.000 0.080 17 43092113 missense variant T/C;G snv 2.5E-03 1.0E-02 2
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs3218674
ATM
1.000 0.120 11 108244860 synonymous variant C/G;T snv 1.1E-02 1.1E-02 2
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs9610
IL10RA ; SMIM35
0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205