Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58064122
GFAP
0.882 0.160 17 44913334 missense variant G/A;C snv 3
rs867657798
TCF4
0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 5
rs9288516
XRCC5
0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs137852972
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 10
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 10
rs4809324
RTEL1 ; RTEL1-TNFRSF6B
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02 7
rs1476157710
WNT10B
0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs4261436
AKAP6
0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43 3
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7