Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2286896
NAB1
1.000 0.080 2 190670850 intron variant T/C snv 0.19 1
rs2287618
ABCB11
1.000 0.080 2 168986299 intron variant T/C snv 0.69 0.73 1
rs2422239 1.000 0.080 2 118271503 intergenic variant G/A snv 0.49 1
rs2422241 1.000 0.080 2 118285460 intergenic variant G/A snv 0.47 1
rs2894450 1.000 0.080 2 222132385 intergenic variant G/A snv 0.56 1
rs3771317
NAB1
1.000 0.080 2 190679236 intron variant T/C;G snv 1
rs41382444
STAT1
1.000 0.080 2 191015488 intron variant C/T snv 4.8E-02 1
rs4675369 1.000 0.080 2 203778471 upstream gene variant A/G snv 0.15 1
rs4952108 1.000 0.080 2 30206869 upstream gene variant C/A;T snv 1
rs4973341 1.000 0.080 2 227795646 intergenic variant C/T snv 0.67 1
rs6749293
LOC107985960
1.000 0.080 2 172302075 intron variant T/C snv 0.12 1
rs974448 1.000 0.080 2 222140595 intergenic variant A/G snv 0.16 1
rs582054
IL12A ; IL12A-AS1
0.882 0.160 3 159992214 intron variant A/C;T snv 5
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35 4
rs1131265
TIMMDC1
0.882 0.200 3 119503609 stop lost G/C snv 0.18 0.18 3
rs1132200
TMEM39A
0.925 0.160 3 119431989 missense variant C/T snv 0.12 0.11 3
rs2293370
TIMMDC1
0.882 0.160 3 119501087 intron variant G/A snv 0.18 3
rs12494314
ARHGAP31
0.925 0.160 3 119403973 intron variant T/C snv 0.15 2
rs1874886
IL12A-AS1
0.925 0.280 3 160011868 non coding transcript exon variant G/A snv 0.41 2
rs4679904 0.925 0.080 3 160623108 intergenic variant C/G;T snv 2
rs485499
LINC01100 ; IL12A-AS1
0.925 0.080 3 160028076 intron variant T/C snv 0.29 2
rs564799
IL12A-AS1
0.925 0.160 3 160011200 intron variant C/T snv 0.33 2
rs6441286
IL12A-AS1
0.925 0.080 3 160011091 intron variant T/G snv 0.36 2
rs668998
IL12A-AS1
0.925 0.120 3 159997764 non coding transcript exon variant G/A snv 0.63 2
rs13097965 1.000 0.080 3 184621969 intergenic variant C/T snv 0.43 1