Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4746201
REEP3
1.000 0.120 10 63562621 intron variant G/A;T snv 2.2E-05; 0.16 1
rs4688011
TIMMDC1
1.000 0.120 3 119508400 intron variant G/A;C snv 0.15 1
rs12046117
VTCN1
1.000 0.120 1 117208743 intron variant C/T snv 0.16 1
rs10128264
ZMIZ1
1.000 0.120 10 79200216 intron variant T/C snv 0.64 1
rs2240337
PADI4
0.925 0.200 1 17347727 intron variant C/T snv 9.5E-02 2
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 3
rs10919563
PTPRC
0.925 0.120 1 198731313 intron variant G/A snv 0.21 3
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 3
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs2348071
ARMH4 ; PSMA3
0.827 0.240 14 58263908 intron variant A/G snv 0.71 5
rs2372536
ATIC
0.827 0.160 2 215325297 missense variant C/G snv 0.33 0.25 5
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 5
rs10931481
STAT4
0.827 0.240 2 191090126 intron variant G/A snv 0.66 5
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21 5
rs6498169
CLEC16A
0.807 0.280 16 11155472 non coding transcript exon variant G/A snv 0.66 6
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs11466018
MEFV
0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 7
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10