Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2488457
AP4B1-AS1 ; PTPN22
0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 5
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs1003706636
NLRP3
1.000 0.120 1 247424639 missense variant T/C snv 1
rs10431961
MMP25
1.000 0.120 16 3050094 synonymous variant C/G;T snv 4.0E-06; 0.32 1
rs11225055
ANGPTL5
1.000 0.120 11 101900702 intron variant T/A;C snv 1
rs12652364 1.000 0.120 5 30835972 intergenic variant G/A;T snv 1
rs2893922
JMJD1C
1.000 0.120 10 63487259 intron variant T/C;G snv 1
rs4395908
CSMD1
1.000 0.120 8 4168122 intron variant C/A;G snv 1
rs4746201
REEP3
1.000 0.120 10 63562621 intron variant G/A;T snv 2.2E-05; 0.16 1
rs6479891
JMJD1C
1.000 0.120 10 63246696 intron variant T/A;C snv 1
rs9414788
JMJD1C
1.000 0.120 10 63296952 intron variant A/C;G;T snv 1
rs953387 1.000 0.120 2 136149600 intergenic variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs11466018
MEFV
0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 7
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs1018981
LOC105375246
1.000 0.120 7 41335525 intergenic variant C/A snv 3.2E-02 1
rs35829419
NLRP3
0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23