Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs144610116
FAM114A1
0.925 0.040 4 38941227 intron variant T/C snv 8.6E-03 2
rs138741635
FHIT
0.925 0.040 3 60942161 intron variant T/A;G snv 2
rs11638352
FRMD5
0.925 0.040 15 44000939 intron variant C/A;G snv 2
rs2733201
FRMD5
0.925 0.040 15 44116203 intron variant T/A;C snv 2
rs148121703
GABRB1
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03 2
rs145044782
GLCCI1
0.925 0.040 7 7995866 intron variant G/A snv 2.9E-02 2
rs3784929
KARS1
0.925 0.160 16 75643129 intron variant A/G snv 0.30 2
rs8053257
KARS1
0.925 0.120 16 75640790 intron variant G/A snv 0.18 2
rs697829
KCNE5
0.925 0.160 X 109623948 3 prime UTR variant G/A snv 2
rs16985615
LOC107985383
1.000 0.040 20 23661790 intron variant T/A;C snv 2
rs4357117
LOC107986540
0.925 0.040 6 66873865 intergenic variant G/T snv 1.7E-02 2
rs151269874
TMEM231
0.925 0.040 16 75549741 intron variant C/T snv 6.2E-03 2
rs57578064
TOMM5
0.925 0.040 9 37590253 intron variant G/A snv 1.9E-02 2
rs190543502
TP53BP1
0.925 0.040 15 43464986 intron variant T/A;C snv 2
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs1967309
ADCY9
0.925 0.080 16 4015582 non coding transcript exon variant A/G snv 0.51 3
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs622064
DNAJB13
0.882 0.240 11 73961529 intron variant C/A snv 0.30 3
rs5940
LOC105373786 ; TFPI
0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02 3
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3