Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs4467099
LOC400499
16 11449038 missense variant C/A;T snv 0.66 1
rs4683336
KRBOX1 ; ACKR2
3 42818461 intron variant C/T snv 0.61 1
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
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
rs7518687
LOC105371604
1 168663745 intergenic variant A/T snv 0.22 1
rs8014067
SYT16
14 62086539 intron variant A/T snv 0.79 1
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs9522267 13 111544020 intergenic variant G/A snv 0.32 1