Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs950881
IL18R1 ; IL1RL1
1.000 0.120 2 102316052 intron variant G/A;T snv 2
rs35597970
MFSD13A ; ACTR1A
1.000 0.120 10 102469300 intron variant -/A delins 0.46 1
rs11668618
MRPL4
1.000 0.120 19 10255220 non coding transcript exon variant C/T snv 0.16 1
rs12509403
NFKB1 ; LOC105377347
1.000 0.120 4 102604193 intron variant C/T snv 0.31 1
rs2472448
ABCA1
1.000 0.120 9 104842226 intron variant C/T snv 0.11 1
rs13217795
FOXO3
0.925 0.120 6 108652895 intron variant C/T snv 0.55 2
rs4713039
SYCP2L
1.000 0.120 6 10906023 synonymous variant A/G snv 0.20 0.15 1
rs887864
CLEC16A
0.925 0.120 16 11065028 intron variant G/A;C;T snv 2
rs17513503 0.882 0.120 5 110810746 intergenic variant C/A;G snv 3
rs2289276
TSLP
0.882 0.160 5 111071809 5 prime UTR variant C/T snv 0.27 3
rs11466749
TSLP
0.925 0.120 5 111076887 3 prime UTR variant A/G snv 0.15 2
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs35350651
ATXN2
1.000 0.120 12 111469627 3 prime UTR variant -/C ins 0.66 1
rs11644510
CLEC16A
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39 2
rs360721
IL18
0.882 0.200 11 112155193 intron variant G/A;C snv 3
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1600249
BLK
0.827 0.280 8 11502129 intron variant G/T snv 0.23 5
rs6898653 0.925 0.120 5 116639960 intergenic variant A/G snv 0.26 2
rs141023293
SIK3
1.000 0.120 11 116902201 intron variant G/A snv 1.5E-02 1
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614