Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047782
TDP2
6 24650503 3 prime UTR variant T/C;G snv 1
rs10484389
CASC15
6 22075033 intron variant C/T snv 6.0E-02 1
rs11025185
NAV2
11 19572259 intron variant G/A snv 2.4E-03 1
rs1432133
GABRG3
15 26983199 intron variant A/G;T snv 1
rs17568725 5 171743637 TF binding site variant C/A snv 0.19 1
rs2174866
LOC107983981
15 53172023 intergenic variant A/T snv 6.2E-02 1
rs3087943
TDP2
6 24650533 3 prime UTR variant A/G snv 0.18 1
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
rs7518687
LOC105371604
1 168663745 intergenic variant A/T snv 0.22 1
rs8014067
SYT16
14 62086539 intron variant A/T snv 0.79 1
rs9522267 13 111544020 intergenic variant G/A snv 0.32 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
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36