Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs4537731 1.000 0.040 11 18047335 upstream gene variant T/C snv 0.48 3
rs77005575 1.000 0.040 6 32611931 intergenic variant T/C snv 2
rs1248696
DLG5
0.807 0.080 10 77856847 missense variant T/A;C snv 0.93 8
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs242924
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.882 0.080 17 45808001 intron variant G/T snv 0.44 3
rs1384936174
NOD2
0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 6
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs2349775
NXPH1
0.851 0.120 7 8678450 intron variant G/A;C snv 6
rs149382949
ANKZF1
1.000 0.040 2 219232579 missense variant G/A;C snv 3.2E-05; 4.0E-06 2
rs750438327
TG
1.000 0.040 8 132888076 missense variant G/A;C snv 7.6E-05 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs199473072
SCN5A
0.827 0.160 3 38613773 missense variant G/A snv 1.2E-05 8.4E-05 5
rs3129891 0.851 0.160 6 32447303 downstream gene variant G/A snv 0.20 5
rs62636489
MIR9898 ; KRT8
0.925 0.040 12 52898860 missense variant G/A snv 7.6E-05 7.0E-06 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15