Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs132630295
RAB9B ; PLP1
1.000 0.080 X 103786682 missense variant C/T snv 1
rs8112449
CDC37
0.925 0.160 19 10409388 intron variant G/A snv 0.31 2
rs733724
HACE1
1.000 0.080 6 104775989 intron variant G/A snv 6.1E-02 1
rs2726518
TET2-AS1 ; TET2
1.000 0.080 4 105252042 intron variant A/C snv 0.63 1
rs6437585
ALCAM
0.882 0.160 3 105367241 5 prime UTR variant C/T snv 9.7E-02 3
rs34926152
ALCAM
1.000 0.080 3 105545332 missense variant G/A;T snv 4.0E-06; 3.5E-02 1
rs11559013
ALCAM
1.000 0.080 3 105575658 3 prime UTR variant G/A;T snv 1
rs11621145
IGHA1
1.000 0.080 14 105706543 intron variant G/A snv 0.49 3
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs12487066
LOC105374027
1.000 0.080 3 106193283 intron variant T/C snv 0.28 2
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs878859113
CD24
0.763 0.360 6 106971734 missense variant G/A snv 0.35 11
rs6622139 1.000 0.080 X 107053120 intergenic variant T/C snv 0.36 1
rs1326656542
LIG4
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs2228315
SELPLG
0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs4774
CIITA
0.807 0.240 16 10906991 missense variant G/C snv 0.30 0.28 7
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1465201414
CLEC16A
1.000 0.080 16 10971132 missense variant A/G snv 8.0E-06 7.0E-06 1
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs8056098
CLEC16A
1.000 0.080 16 11044955 intron variant G/A;C;T snv 1
rs11860603
CLEC16A
1.000 0.080 16 11071160 intron variant T/C snv 0.41 1