Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs737337
DOCK6
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 6
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs535039125
CYP2B6
0.851 0.040 19 41004380 missense variant C/T snv 1.1E-04 1.3E-04 5
rs1739843
HSPB7
0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs61661343
LMNA
0.851 0.040 1 156130687 missense variant T/C snv 4
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs10927887
CLCNKA
0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs11006544
LOC107984235
1.000 0.040 10 59510886 intergenic variant T/C snv 7.3E-03 3
rs11110004
ANKS1B
1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03 3
rs112434206 1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03 3
rs113235453
NUBPL
1.000 0.040 14 31849939 intron variant A/G snv 3.5E-02 3
rs114821210 1.000 0.040 5 166089843 intergenic variant C/A snv 6.0E-03 3
rs12362161 1.000 0.040 11 98834502 intergenic variant C/A;G snv 3
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs1258130495
EDNRA
0.882 0.040 4 147485727 missense variant G/A snv 3
rs1303946678
CYP2D6 ; NDUFA6-DT
0.925 0.040 22 42126851 missense variant C/G snv 3
rs139130723 1.000 0.040 6 14411553 intergenic variant A/G snv 4.4E-03 3
rs142803096 1.000 0.040 6 14420151 intergenic variant G/C snv 4.4E-03 3
rs144303414 1.000 0.040 18 48509413 intergenic variant A/C snv 1.5E-02 3
rs148133894 1.000 0.040 16 24584678 intergenic variant T/C snv 2.4E-03 3
rs149322277
CA5A
1.000 0.040 16 87925065 intron variant C/T snv 5.6E-03 3