Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs3753793
CCN1 ; DDAH1
0.851 0.240 1 85580205 upstream gene variant A/C snv 0.26 4
rs12756618 1.000 0.160 1 85587205 downstream gene variant C/T snv 4.5E-02 1
rs1378228
DDAH1
1.000 0.160 1 85570890 intron variant G/C;T snv 1
rs6682848
DDAH1
1.000 0.160 1 85572793 intron variant A/C snv 0.89 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs733618
CTLA4
0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 12
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs16840252
CTLA4
0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
rs11675434
TPO
0.827 0.240 2 1404043 non coding transcript exon variant C/T snv 0.39 5
rs3917368 1.000 0.160 2 112825205 upstream gene variant C/T snv 0.29 1
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs13143866
IL21 ; IL21-AS1
0.851 0.200 4 122619603 intron variant G/A snv 0.24 4
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs40401
IL3 ; LOC105379174
0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33 8
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 7
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5