Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8014067
SYT16
14 62086539 intron variant A/T snv 0.79 1
rs1432133
GABRG3
15 26983199 intron variant A/G;T snv 1
rs2174866
LOC107983981
15 53172023 intergenic variant A/T snv 6.2E-02 1
rs4467099
LOC400499
16 11449038 missense variant C/A;T snv 0.66 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs10853728 0.851 0.160 19 39254506 downstream gene variant C/A;G;T snv 5
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88