Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3136558
IL1B
1.000 2 112833698 intron variant A/G snv 0.21 4
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs371194629
HLA-G
0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs397516808
PTPN11
12 112446327 synonymous variant A/G snv 1.6E-05 1.4E-05 1
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs486907
RNASEL
0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs7269320
MAVS
20 3865750 missense variant C/T snv 0.16 0.21 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06 2
rs781522558
STAT2
1.000 12 56346844 stop gained G/C;T snv 4.0E-06 2
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60