Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs434082
SLC8A1
0.925 0.160 2 40257934 intron variant C/T snv 0.14 3
rs11893826
SLC8A1
0.925 0.160 2 40337507 intron variant G/A snv 0.27 2
rs274068
SLC5A11
0.925 0.160 16 24887651 intron variant C/A snv 0.74 2
rs11057864
SCARB1
0.925 0.160 12 124851404 intron variant C/A snv 6.5E-02 2
rs114580964
PRRC2A
1.000 0.160 6 31636736 missense variant C/A;T snv 3.4E-03 1.4E-03 1
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs3792192
PLA2R1
0.925 0.160 2 160030364 intron variant G/A snv 0.35 2
rs329498
PELI1
0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 3
rs1635564
PADI4
0.925 0.160 1 17357031 intron variant T/A;G snv 2
rs8012283
NIN
0.925 0.160 14 50767442 intron variant A/G snv 0.23 2
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs2157257
MYH9
1.000 0.160 22 36312293 intron variant A/G snv 0.52 1
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193