Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11225055
ANGPTL5
1.000 0.120 11 101900702 intron variant T/A;C snv 1
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs6498169
CLEC16A
0.807 0.280 16 11155472 non coding transcript exon variant G/A snv 0.66 6
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2488457
AP4B1-AS1 ; PTPN22
0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs12046117
VTCN1
1.000 0.120 1 117208743 intron variant C/T snv 0.16 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs757278
CTTNBP2
1.000 0.120 7 117737591 intron variant G/T snv 0.44 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs4688011
TIMMDC1
1.000 0.120 3 119508400 intron variant G/A;C snv 0.15 1
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs16939895
PTPN2
1.000 0.120 18 12821904 intron variant G/A snv 0.17 1