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
rs781522558
STAT2
1.000 12 56346844 stop gained G/C;T snv 4.0E-06 2
rs1336795098
NUP214
9 131127544 synonymous variant A/G snv 7.0E-06 1
rs1364498756
IRF9
14 24166173 missense variant G/A snv 1
rs139226823
CXCR3
X 71616597 missense variant C/G;T snv 5.5E-06; 5.7E-04 1
rs397516808
PTPN11
12 112446327 synonymous variant A/G snv 1.6E-05 1.4E-05 1
rs7269320
MAVS
20 3865750 missense variant C/T snv 0.16 0.21 1
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06 2
rs12487066
LOC105374027
1.000 0.080 3 106193283 intron variant T/C snv 0.28 2
rs1480480967
IFNA13
1.000 0.080 9 21367884 missense variant C/T snv 4.0E-06 2
rs17886084
MMP1 ; WTAPP1
1.000 0.080 11 102799765 intron variant C/- delins 2
rs1818879 0.827 0.120 7 22733108 downstream gene variant G/A;C snv 7
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs179363879
AIRE
0.925 0.160 21 44286092 missense variant T/C snv 3
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
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
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs371194629
HLA-G
0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs486907
RNASEL
0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15