Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62141163 1.000 0.040 2 31440248 regulatory region variant G/A snv 7.6E-02 2
rs6503695
STAT3
0.925 0.040 17 42347515 intron variant T/C snv 0.33 2
rs7649970
PPARG
1.000 0.040 3 12350773 intron variant C/T snv 0.14 2
rs1057613
MTTP
1.000 0.040 4 99583828 3 prime UTR variant G/A snv 0.60 1
rs11166927
TRAPPC9
1.000 0.040 8 139784177 intron variant T/C snv 0.39 1
rs11235972
UCP3
1.000 0.040 11 74006029 intron variant G/A snv 0.21 1
rs117542855 1.000 0.040 11 1635713 regulatory region variant C/G;T snv 3.1E-02 1
rs11794552
LOC105376299 ; PLPP7
1.000 0.040 9 131344938 intron variant C/T snv 0.15 1
rs12373751
ERBB4
1.000 0.040 2 212072166 intron variant T/C snv 0.62 1
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
rs13428113
LOC107985940 ; INSIG2
1.000 0.040 2 118089309 intron variant T/C snv 0.51 1
rs139051
PNPLA3
1.000 0.040 22 43928796 intron variant A/G snv 0.56 0.59 1
rs1412189378
MTTP
1.000 0.040 4 99583404 missense variant C/A snv 1
rs143392071
PNPLA3
1.000 0.040 22 43933050 missense variant A/G snv 7.2E-04 2.1E-04 1
rs1492100
AGTR1
1.000 0.040 3 148719640 intron variant T/A snv 0.34 1
rs17120035
APOA5
1.000 0.040 11 116793135 upstream gene variant C/T snv 6.4E-02 1
rs1800804
MTTP
1.000 0.040 4 99574660 intron variant T/C snv 0.26 1
rs1805074
DMGDH
1.000 0.040 5 79028529 missense variant A/G snv 0.27 0.33 1
rs1858999
GATAD2A
1.000 0.040 19 19386860 intron variant C/G snv 0.56 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
rs200848339
TLR4
1.000 0.040 9 117713001 synonymous variant A/G snv 2.4E-05 1
rs2073082
SAMM50 ; PNPLA3
1.000 0.040 22 43964127 intron variant G/A snv 0.18 1