Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs33996649
PTPN22 ; AP4B1-AS1
0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 8
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 8
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs1333062
ITLN1
0.807 0.200 1 160876494 downstream gene variant T/C;G snv 6
rs16841904
DENND1B
0.807 0.160 1 197732862 intron variant C/T snv 0.18 6
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 6
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 6