Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3092920 0.925 0.160 X 136661832 downstream gene variant G/T snv 0.23 2
rs315951
IL1RN
0.925 0.160 2 113133009 3 prime UTR variant C/G snv 0.34 2
rs3784929
KARS1
0.925 0.160 16 75643129 intron variant A/G snv 0.30 2
rs559110055
ABCA1
0.925 0.160 9 104840491 missense variant A/G snv 4.0E-06 2
rs697829
KCNE5
0.925 0.160 X 109623948 3 prime UTR variant G/A snv 2
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs1187513719
CYP2C19
0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 4
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 4
rs2029253
ALOX5
0.925 0.200 10 45396036 intron variant A/G snv 0.37 3
rs2046934
MED12L ; P2RY12
0.882 0.200 3 151339854 intron variant G/A;C snv 3
rs2240419
HDAC9
0.925 0.200 7 18935566 intron variant T/A;C snv 3
rs2389995
HDAC9
0.925 0.200 7 18933395 intron variant A/G snv 6.0E-02 3
rs501192
CASP1
0.925 0.200 11 105029658 splice region variant C/T snv 0.17 0.15 3
rs2298212
TNFRSF4
0.925 0.200 1 1211917 intron variant G/A snv 8.3E-02 8.0E-02 2
rs33977706
RMI2 ; SOCS1 ; LOC105371082
0.925 0.200 16 11256298 intron variant C/A;G;T snv 2
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs4809960
CYP24A1
0.807 0.240 20 54169534 intron variant T/C snv 0.20 8
rs11573156
PLA2G2A
0.882 0.240 1 19979653 5 prime UTR variant G/C snv 0.19 5
rs4769874
ALOX5AP
0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs4986893
CYP2C19
0.827 0.240 10 94780653 stop gained G/A snv 5.4E-03 1.5E-03 5
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4