Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs17375018
C1orf141 ; IL23R
0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39 5
rs6841698 0.882 0.080 4 38760093 upstream gene variant G/A snv 0.36 4
rs1805110
TGFBR3
0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 3
rs2358820
VTCN1
1.000 0.040 1 117169289 intron variant G/A snv 5.3E-02 1
rs397514601
CAPN5
0.882 0.040 11 77115423 missense variant G/A;T snv 4.0E-06 3
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs7565639
PDCD1 ; LOC105373977
0.882 0.160 2 241854911 intron variant T/A;C snv 3
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4
rs2287987
ERAP1
0.882 0.120 5 96793832 missense variant T/C snv 0.15 0.16 3
rs6710479
LOC105373977 ; PDCD1
0.882 0.200 2 241855866 intron variant T/C snv 0.51 3
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10