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
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs387906350
BCL10
0.882 0.120 1 85267830 frameshift variant A/-;AA delins 3
rs928883
MIR155HG
0.882 0.160 21 25571713 intron variant A/G snv 0.83 3
rs11797
TREX1 ; ATRIP-TREX1 ; ATRIP
0.925 0.160 3 48467186 synonymous variant T/C snv 0.63 2
rs587776630
BCL10
1.000 0.120 1 85270800 frameshift variant -/T delins 1
rs587776631
BCL10
1.000 0.120 1 85270619 frameshift variant T/- delins 1