Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1955513
AKAP6
0.925 0.120 14 32706736 intron variant T/G snv 0.11 2
rs9787692 1.000 0.120 10 8603200 intergenic variant T/G snv 0.30 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1799950
BRCA1
0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13
rs16949649
NME1 ; NME1-NME2
0.776 0.200 17 51152947 upstream gene variant T/C snv 0.39 12
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 5
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 5
rs192876988
LOC105377300
0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 4
rs9909104
SHMT1
0.882 0.200 17 18344707 intron variant T/C snv 0.30 4
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs114972508
EGFR ; LOC105375284
0.925 0.120 7 55020815 intron variant T/C snv 1.4E-02 2
rs17106154
RAD51B
0.925 0.120 14 68694457 non coding transcript exon variant T/C snv 7.8E-02 2
rs7053448
F8
0.925 0.120 X 154964936 intron variant T/C snv 0.15 2
rs7572644
BABAM2
0.925 0.120 2 28097166 intron variant T/C snv 0.21 2
rs9609538
BPIFC ; RTCB
0.925 0.120 22 32413845 upstream gene variant T/C snv 0.34 2
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs4758680
LRRC43
0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs2303428
MSH2
0.776 0.240 2 47476361 splice region variant T/A;C;G snv 4.0E-06; 0.12 9
rs1596797
MUC16
0.925 0.120 19 8977341 missense variant T/A;C;G snv 2.0E-05; 4.0E-06; 0.74 2
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 3
rs80357796
BRCA1
0.752 0.240 17 43094464 frameshift variant T/- del 11