Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs1183194405
F2
0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs2066842
NOD2
0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14