Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs1051861187
ABCB4
0.827 0.080 7 87409385 missense variant A/G snv 6
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs5743314
TLR3
0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs104894630
SCO1
0.882 0.120 17 10692805 missense variant G/A snv 4
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs1879026
TLR3
1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs35724
NR1H4
0.925 0.040 12 100561600 intron variant C/G snv 0.52 3
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs111200466
TLR2
1.000 0.080 4 153684312 5 prime UTR variant CGGCTGCTCGGCGTTCTCTCAGG/- delins 0.17 2
rs121434622
FMR1
1.000 0.080 X 147936534 missense variant T/A snv 2
rs1420111973
TLR4
1.000 0.080 9 117712527 synonymous variant T/C snv 7.0E-06 2
rs4849133 2 112923864 downstream gene variant C/A;T snv 2
rs762623
CDKN1A ; DINOL
1.000 0.160 6 36677689 non coding transcript exon variant G/A snv 0.12 2
rs1281032650
LNPEP
5 96979168 missense variant A/G snv 1
rs3116996 6 33130187 downstream gene variant T/A snv 0.13 1
rs7314777
LOC105369818
12 68256855 upstream gene variant T/C snv 0.19 1
rs751703423
AIMP2 ; EIF2AK1
7 6023410 missense variant G/A;C snv 1
rs868564661
FGFR2
10 121487415 missense variant G/A snv 1
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5