Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13415583
AFF3
1.000 0.120 2 100147625 intron variant T/G snv 0.37 1
rs941576
MEG3
1.000 0.120 14 100839708 intron variant A/G snv 0.45 1
rs56994090
MEG3
1.000 0.120 14 100840110 intron variant T/A;C snv 1
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs879228335
MOK
1.000 0.120 14 102229329 missense variant T/C snv 1
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs28641753 0.925 0.160 3 104256574 intergenic variant C/T snv 4.5E-02 2
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs9810233 0.925 0.200 3 105292046 intergenic variant A/G snv 0.25 2
rs1223438908
CBLB
1.000 0.120 3 105681480 missense variant T/G snv 4.0E-06 2
rs752455542
CBLB
1.000 0.120 3 105681740 missense variant T/G snv 4.0E-06 2
rs3772534
CBLB
1.000 0.120 3 105702190 synonymous variant C/T snv 3.1E-02 2.0E-02 1
rs1950942 1.000 0.120 14 105861856 upstream gene variant A/C;G snv 1
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 2
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs1460002897
SLC26A3
1.000 0.120 7 107793769 missense variant T/C snv 4.0E-06 1
rs11074932
LOC105371080 ; CIITA
1.000 0.120 16 10874479 intron variant T/A;C snv 1
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14