Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 5
rs72796353
NOD2
0.882 0.080 16 50712383 3 prime UTR variant A/C snv 1.3E-02 1.4E-02 5
rs12948909
CAVIN1
0.925 0.120 17 42418584 intron variant A/C snv 0.24 3
rs2382817
PNKD ; TMBIM1
0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 3
rs6017342
LINC01620
0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 3
rs2647087 1.000 0.040 6 32713272 upstream gene variant A/C snv 0.29 2
rs7165170
CRTC3-AS1 ; CRTC3
1.000 0.040 15 90638257 non coding transcript exon variant A/C snv 0.26 2
rs2395022
KPNA7
7 99152756 intergenic variant A/C snv 0.93 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs16910526
CLEC7A ; LOC105369655
0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs527892258
NOD2
0.925 0.040 16 50723350 missense variant A/C;G snv 1.7E-04; 4.4E-05 3
rs10051722 1.000 0.040 5 130768383 intron variant A/C;G snv 2
rs4149570
TNFRSF1A
0.752 0.360 12 6342424 upstream gene variant A/C;G;T snv 11
rs10142466 14 68805067 intergenic variant A/C;G;T snv 1
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99