Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1351687973
TP73
0.925 0.120 1 3731497 missense variant G/A snv 1.6E-05 3
rs1555525126
TP53
0.925 0.120 17 7673749 missense variant T/C snv 3
rs535311760
TP73
0.925 0.120 1 3730979 missense variant G/A snv 1.2E-05; 8.2E-06 3
rs867830180
TNFRSF6B ; RTEL1 ; RTEL1-TNFRSF6B
0.925 0.120 20 63695147 missense variant G/A;T snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs1257715362
MAPK10 ; ARHGAP24
0.925 0.120 4 85995065 missense variant A/G snv 7.0E-06 3
rs138228187
TIRAP
0.925 0.120 11 126292650 missense variant C/T snv 4.0E-05 1.4E-05 3
rs867329357
ERCC5 ; BIVM-ERCC5
0.925 0.120 13 102872275 missense variant G/A snv 4.0E-06 4.9E-05 3
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs2274084
GJB2
0.882 0.240 13 20189503 missense variant C/T snv 5.4E-02 2.2E-02 6
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs11466782
ADAM19
0.925 0.120 5 157494947 intron variant A/G snv 0.10 3
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs751837
CDC42BPB
0.882 0.120 14 103018488 intron variant T/C snv 0.23 4
rs10190751
CFLAR-AS1 ; CFLAR
0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs6676671
IL19
0.882 0.160 1 206779403 intron variant T/A snv 0.32 4
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs708486
PTGDR
0.925 0.120 14 52274253 intron variant A/G snv 0.35 3
rs10494879
IL19
0.925 0.120 1 206778859 intron variant C/A;G snv 0.36 3