Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 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
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
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
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs16910526
CLEC7A ; LOC105369655
0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12