Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs773862672
MTOR
0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs9610
IL10RA ; SMIM35
0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs104893626
CXCR4 ; LOC112268426
0.827 0.280 2 136114915 stop gained G/C snv 11
rs539846
BMF
1.000 0.120 15 40105735 intron variant G/C;T snv 2
rs1053023
STAT3
0.882 0.120 17 42313598 3 prime UTR variant T/A;C snv 4
rs355689
LOC105377296 ; CXCL13
1.000 0.040 4 77586643 intron variant T/A;C snv 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
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
rs3789607
AP4B1-AS1 ; PTPN22
1 113823812 intron variant T/C snv 0.21 1
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2227945
BRCA1
1.000 0.080 17 43092113 missense variant T/C;G snv 2.5E-03 1.0E-02 2