Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs1966265
FGFR4
0.827 0.160 5 177089630 missense variant G/A;T snv 0.25 8
rs2011077
FGFR4
0.807 0.080 5 177094455 intron variant C/T snv 0.19 8
rs3093030
ICAM4 ; ICAM1
0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34 6
rs784567
TARBP2 ; MAP3K12
0.851 0.320 12 53500681 non coding transcript exon variant G/A;T snv 5
rs78303930
NES
0.925 0.120 1 156670593 missense variant C/A;G snv 4.0E-06; 2.4E-03 4
rs16970849
TMC8
0.882 0.080 17 78137827 intron variant G/A;T snv 0.11; 4.0E-06 4
rs2290907
TNRC6C
0.882 0.080 17 78097596 intron variant T/C snv 0.23 4
rs7708357 1.000 0.080 5 177104771 intergenic variant A/G snv 0.58 2
rs311678
CGAS
1.000 0.040 6 73425293 synonymous variant C/T snv 0.71 0.72 2
rs6052130
MAVS
1.000 0.040 20 3863021 intron variant C/A snv 9.5E-02 2
rs12435483
TRAF3
1.000 0.080 14 102865271 intron variant C/T snv 0.14 2