Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs547984 0.882 0.040 1 237933586 intergenic variant A/C snv 0.60 3
rs16958477
LOXL1-AS1 ; LOXL1
0.925 0.040 15 73926125 5 prime UTR variant A/C snv 0.33 2
rs113432289
RAPGEF5
1.000 0.040 7 22253498 intron variant A/C snv 3.3E-03 1
rs2024211 1.000 0.040 7 116512971 downstream gene variant A/C snv 0.27 1
rs28500712
AFAP1
1.000 0.040 4 7894486 intron variant A/C;G snv 2
rs28795989
AFAP1
1.000 0.040 4 7889818 intron variant A/C;G snv 2
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs17752199 0.925 0.040 6 51542050 upstream gene variant A/C;G;T snv 3
rs74315331
MYOC ; MYOCOS
0.882 0.040 1 171636010 missense variant A/C;T snv 3
rs190298731 1.000 0.040 6 148738155 intergenic variant A/C;T snv 1
rs2437812
LOC105376196
1.000 0.040 9 104930920 upstream gene variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 15
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs74315328
MYOC ; MYOCOS
0.807 0.120 1 171636131 missense variant A/G snv 6
rs267606929
OPTN
0.827 0.120 10 13132098 missense variant A/G snv 5
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs9913911
GAS7
0.925 0.040 17 10127866 intron variant A/G snv 0.32 4
rs1579050
FMNL2
0.925 0.040 2 152508013 intron variant A/G snv 0.42 3
rs2745572
LOC102723944
0.925 0.040 6 1548134 intergenic variant A/G snv 0.31 3
rs284489
ZFPM2
0.882 0.080 8 104945792 intron variant A/G snv 0.45 3