Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs6050
FGA
0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 10
rs7422339
CPS1
1.000 0.080 2 210675783 missense variant C/A snv 5
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 4
rs16844401
HGFAC
1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs10157379
NLRP3
1 247442297 intron variant C/G;T snv 3
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 3
rs11242111
LINC02863 ; IRF1-AS1
5 132420366 intron variant A/G;T snv 3
rs12915708
SPPL2A
15 50756405 intron variant G/A;C snv 3
rs1476698
FARP2
2 241357034 intron variant A/G;T snv 3
rs17690122 5 132532143 intron variant A/G;T snv 3
rs4508864 4 154560137 upstream gene variant C/G;T snv 3
rs511154 3 136232079 intergenic variant A/G;T snv 3
rs7464572
MIR661 ; PLEC
8 143946999 intron variant C/A;G snv 3
rs7588285
COLEC11
2 3600596 intron variant C/G;T snv 3
rs7896783
JMJD1C
10 63402393 intron variant G/A;C snv 3
rs11230201
MS4A4E ; MS4A4A
1.000 0.080 11 60229521 intron variant C/G;T snv 2
rs2801231 1.000 0.080 X 122083259 intergenic variant T/A;C;G snv 2
rs35489971
CD300LF ; RAB37
1.000 0.040 17 74704804 missense variant A/G;T snv 0.73 2
rs7012814 8 9315848 intron variant G/A;T snv 2
rs1012793
IRF1-AS1
5 132445653 intron variant G/A;C snv 1