Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2235312
APLN
0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs41273215
PEAR1
0.882 0.160 1 156912167 intron variant C/T snv 0.13 3
rs622064
DNAJB13
0.882 0.240 11 73961529 intron variant C/A snv 0.30 3
rs11638352
FRMD5
0.925 0.040 15 44000939 intron variant C/A;G snv 2
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02 2
rs12766939
CUBN
0.925 0.160 10 17031136 intron variant A/G snv 0.23 2
rs138741635
FHIT
0.925 0.040 3 60942161 intron variant T/A;G snv 2
rs144610116
FAM114A1
0.925 0.040 4 38941227 intron variant T/C snv 8.6E-03 2
rs145044782
GLCCI1
0.925 0.040 7 7995866 intron variant G/A snv 2.9E-02 2
rs147204125
ACOT6
0.925 0.040 14 73609035 intron variant A/G snv 9.8E-03 2
rs148121703
GABRB1
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03 2
rs151269874
TMEM231
0.925 0.040 16 75549741 intron variant C/T snv 6.2E-03 2
rs16985615
LOC107985383
1.000 0.040 20 23661790 intron variant T/A;C snv 2
rs190543502
TP53BP1
0.925 0.040 15 43464986 intron variant T/A;C snv 2
rs2733201
FRMD5
0.925 0.040 15 44116203 intron variant T/A;C snv 2
rs35610040
CST3
1.000 0.040 20 23635832 intron variant T/C snv 0.19 2
rs3784929
KARS1
0.925 0.160 16 75643129 intron variant A/G snv 0.30 2
rs57578064
TOMM5
0.925 0.040 9 37590253 intron variant G/A snv 1.9E-02 2
rs8053257
KARS1
0.925 0.120 16 75640790 intron variant G/A snv 0.18 2
rs117038461
CASTOR3
1.000 0.040 7 100243731 intron variant C/T snv 1.5E-02 1
rs140104968 1.000 0.040 7 99946004 intron variant C/T snv 1.5E-02 1
rs147642358
ARPC1A
1.000 0.040 7 99335136 intron variant G/A;T snv 1
rs188845491
CYP3A51P ; CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
1.000 0.040 7 99689016 intron variant C/T snv 2.5E-04 1
rs6139591
SLC23A2
1.000 0.040 20 4970713 intron variant G/A snv 0.40 1