Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2854117
APOC3
0.851 0.200 11 116829426 upstream gene variant T/A;C snv 6
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs5854292
EGFEM1P
0.851 0.080 3 168680960 intron variant AA/-;A;AAA delins 5
rs1131580
TNFSF10
0.882 0.160 3 172505830 3 prime UTR variant A/C;G;T snv 4
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs2235543
HSD11B1-AS1 ; HSD11B1
0.925 0.080 1 209687323 intron variant T/A;C snv 4
rs3772622
AGTR1
0.851 0.080 3 148717966 intron variant T/A;C snv 4
rs1057156731
LMNA
0.925 0.120 1 156137730 missense variant T/A snv 3
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs2638360
AGTR1
0.925 0.080 3 148710569 intron variant G/A;T snv 3
rs3747206
PNPLA3
0.882 0.160 22 43928850 synonymous variant C/T snv 3
rs6850524
CLOCK
0.925 0.080 4 55515830 intron variant C/G;T snv 3
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs1420472625
MBOAT7
0.925 0.040 19 54178800 missense variant G/C snv 2
rs2070667
APOC3
1.000 0.040 11 116830953 intron variant G/A;C;T snv 2
rs2710833
DDX60L ; LOC107986198
0.925 0.080 4 168488807 intron variant T/A;C snv 2
rs343064 0.925 0.080 7 35515178 upstream gene variant C/G;T snv 2
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
rs12565406
HSD11B1 ; HSD11B1-AS1
1.000 0.040 1 209687741 intron variant G/A;T snv 1
rs1292932521
GGTLC3
1.000 0.040 22 18517476 missense variant C/T snv 1
rs13306741
RAI1 ; SREBF1
1.000 0.040 17 17811708 3 prime UTR variant C/A;T snv 4.3E-03; 7.4E-06 1
rs1412189378
MTTP
1.000 0.040 4 99583404 missense variant C/A snv 1
rs1881396
ZNF512
1.000 0.040 2 27621734 3 prime UTR variant T/A;G snv 1
rs1953124 1.000 0.040 13 65771915 regulatory region variant C/A;G;T snv 1