Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs10750097
APOA5
1.000 0.040 11 116793324 upstream gene variant G/A;C snv 6
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs4808199
GATAD2A ; MIR640
1.000 0.040 19 19434290 intron variant G/A;T snv 0.19 5
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 3
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 3
rs12137855
LYPLAL1
0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs206833 1.000 0.040 2 31485750 intergenic variant G/A snv 0.17 3
rs2235776
SAMM50
0.925 0.040 22 43982119 intron variant C/T snv 0.24 3
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs2294918
PNPLA3
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs72563732
ADIPOQ-AS1 ; ADIPOQ
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs74315468
ARSA
0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs11820744
OSBPL5 ; LOC107987158
1.000 0.040 11 3147308 intron variant C/T snv 0.23 2
rs139271658
PTPRD
1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02 2
rs1420472625
MBOAT7
0.925 0.040 19 54178800 missense variant G/C snv 2
rs17618244
KLB
0.925 0.040 4 39446909 missense variant G/A snv 0.18 0.16 2
rs2070667
APOC3
1.000 0.040 11 116830953 intron variant G/A;C;T snv 2
rs2073080
PARVB ; SAMM50
0.925 0.040 22 43998522 intron variant C/T snv 0.20 2
rs2236212
ELOVL2
1.000 0.040 6 10994782 intron variant G/C snv 0.39 2
rs2980888 1.000 0.040 8 125495066 intron variant T/C snv 0.76 2
rs3761472
SAMM50
0.925 0.040 22 43972242 missense variant A/G snv 0.21 0.18 2
rs6006473
PARVB ; SAMM50
0.925 0.040 22 43997195 intron variant C/T snv 0.47 2