Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9508835
ALOX5AP
1.000 0.120 13 30760561 intron variant C/A snv 0.23 1
rs580253
CASP1
1.000 0.120 11 105029761 synonymous variant G/A snv 0.17 0.15 1
rs11086998
CD40
1.000 0.120 20 46128885 missense variant C/G;T snv 2.2E-02 1
rs5369
EDN1
1.000 0.120 6 12294025 synonymous variant A/G snv 0.90 0.88 1
rs4661012
PEAR1
1.000 0.120 1 156915699 3 prime UTR variant T/G snv 0.36 1
rs1208732776
THPO ; CHRD
1.000 0.120 3 184378252 missense variant G/A snv 7.0E-06 1
rs3092920 0.925 0.160 X 136661832 downstream gene variant G/T snv 0.23 2
rs6141803 1.000 0.120 20 32752550 TF binding site variant T/C snv 0.13 2
rs559110055
ABCA1
0.925 0.160 9 104840491 missense variant A/G snv 4.0E-06 2
rs12766939
CUBN
0.925 0.160 10 17031136 intron variant A/G snv 0.23 2
rs3087459
EDN1
0.925 0.160 6 12289406 upstream gene variant A/C snv 0.20 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
rs697829
KCNE5
0.925 0.160 X 109623948 3 prime UTR variant G/A snv 2
rs33977706
RMI2 ; SOCS1 ; LOC105371082
0.925 0.200 16 11256298 intron variant C/A;G;T snv 2
rs2298212
TNFRSF4
0.925 0.200 1 1211917 intron variant G/A snv 8.3E-02 8.0E-02 2
rs3092952 0.925 0.160 X 136644791 upstream gene variant A/G snv 0.29 3
rs676457
ABO
1.000 0.120 9 133270797 intron variant T/A snv 3
rs2029253
ALOX5
0.925 0.200 10 45396036 intron variant A/G snv 0.37 3
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs501192
CASP1
0.925 0.200 11 105029658 splice region variant C/T snv 0.17 0.15 3
rs2762939
CYP24A1
0.925 0.160 20 54164712 intron variant G/C;T snv 3
rs622064
DNAJB13
0.882 0.240 11 73961529 intron variant C/A snv 0.30 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