Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17758761
ANKFN1
1.000 0.080 17 55977164 intron variant A/C snv 4.1E-02 2
rs1252641479
ARHGEF7
1.000 0.040 13 111300800 missense variant T/G snv 4.0E-06 2
rs11204735
ARNT
1.000 0.080 1 150869191 intron variant T/C snv 0.41 2
rs1223438908
CBLB
1.000 0.120 3 105681480 missense variant T/G snv 4.0E-06 2
rs2305035
CBLB
1.000 0.080 3 105720182 synonymous variant G/A snv 0.22 0.21 2
rs752455542
CBLB
1.000 0.120 3 105681740 missense variant T/G snv 4.0E-06 2
rs201909740
CD28
1.000 0.040 2 203734889 missense variant G/A snv 4.0E-06 1.4E-05 2
rs761234173
CDH13
1.000 0.040 16 83783345 missense variant G/A snv 4.0E-06 2
rs786204847
DDX58
1.000 9 32488039 missense variant T/G snv 2
rs10892286
DDX6
11 118771376 intron variant A/C snv 0.17 2
rs11984075
ELMO1
7 37397251 intron variant A/G snv 0.14 2
rs140101069
GLIS3
1.000 0.120 9 3828342 missense variant G/A snv 3.2E-04 8.4E-05 2
rs7538427
GTF2B
1.000 0.080 1 88873739 intron variant C/T snv 0.93 2
rs1772408
IFI16
1 159035859 intron variant A/G;T snv 2
rs2893008
IL21-AS1
4 122631659 intron variant A/G snv 5.1E-02 2
rs148038936
ITGB2 ; LOC107987303
1.000 0.080 21 44910354 missense variant G/A;C snv 2.4E-05; 1.6E-04 2
rs4288027
KIAA1109
4 122262050 intron variant A/C;G snv 0.13 2
rs4374642
KIAA1109
4 122179956 intron variant T/C snv 0.13 2
rs7678445
KIAA1109
4 122361617 intron variant G/A;T snv 2
rs2737713
LGALS8 ; LOC107985367
1.000 0.120 1 236537507 missense variant T/A snv 2
rs10460003
LINC01882
18 12747013 intron variant C/T snv 0.15 2
rs11043097
LINC02752
11 11114248 intron variant T/C snv 0.15 2
rs1517440
LOC105373895
1.000 0.080 2 220589153 intron variant T/C;G snv 2
rs9295089
LOC105378083 ; TAGAP
6 159042932 non coding transcript exon variant T/C snv 0.20 2
rs200395694
MEF2D
1.000 0.080 1 156480799 intron variant G/A;C;T snv 2.7E-05; 1.2E-04; 1.6E-03 2