Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs12342
ADIPOR2
0.851 0.240 12 1787714 3 prime UTR variant C/A;T snv 4
rs3754701
RAMP1
0.882 0.120 2 237858561 upstream gene variant A/C;T snv 4
rs7590387 0.882 0.120 2 237913557 downstream gene variant G/A;C snv 3
rs2238634
TBXA2R
0.925 0.200 19 3604731 intron variant A/C;T snv 2
rs750272074
ROS1
1.000 0.120 6 117362705 synonymous variant A/G snv 4.0E-06 2
rs768963
CACTIN
0.925 0.120 19 3615409 non coding transcript exon variant G/A;C snv 2
rs1044006
NOTCH3
1.000 0.120 19 15174241 synonymous variant T/A;C snv 0.86 1
rs1207570776
DNAJC10
1.000 0.120 2 182757711 missense variant A/G snv 1
rs2270226
RBPJ
1.000 0.120 4 26415514 missense variant T/A;C;G snv 0.57 1
rs4944832
P2RY2
1.000 0.120 11 73238127 upstream gene variant G/A;T snv 1
rs56095120
SMTN
1.000 0.120 22 31100540 intron variant T/A;C snv 1
rs755403632
BMS1
1.000 0.120 10 42792991 missense variant C/G;T snv 4.0E-06; 4.0E-06 1
rs774320676
CTSS
1.000 0.120 1 150750091 missense variant A/T snv 4.0E-06 1
rs928508030
CTSS
1.000 0.120 1 150765698 splice region variant G/A snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs755703581
PDX1
0.925 0.120 13 27920295 missense variant G/A snv 2.3E-05 7.0E-06 3
rs121918474
PROS1
0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 11
rs1801273
FABP1
0.925 0.200 2 88126256 missense variant C/T snv 1.2E-05 2.1E-05 3
rs55951658
CYP3A4
0.827 0.200 7 99770202 missense variant T/A;C snv 4.1E-04 9.8E-05 7
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3731245
CDKN2A
0.925 0.120 9 21972446 intron variant C/T snv 6.6E-03 2
rs3789683
F3
0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 3
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26