Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1718119
LOC105370032 ; P2RX7
0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs1372834938
KIDINS220
0.763 0.280 2 8812465 missense variant G/C snv 4.2E-06 12
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs549908
IL18
0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs1554286
IL19 ; IL10
0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs2522137
MSI1
0.827 0.120 12 120342128 3 prime UTR variant T/A;C;G snv 7
rs1800870
ALDH3A2
0.851 0.200 17 19649164 intron variant C/T snv 5
rs7958311
P2RX7 ; LOC105370032
0.851 0.160 12 121167552 missense variant G/A;C snv 0.25; 4.0E-06 5
rs4988453
MYD88 ; ACAA1
0.851 0.200 3 38137763 upstream gene variant C/A;T snv 4
rs2393799
P2RX7 ; LOC105370032
0.882 0.200 12 121132209 upstream gene variant C/A;T snv 3