Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11820744
OSBPL5 ; LOC107987158
1.000 0.040 11 3147308 intron variant C/T snv 0.23 2
rs12152703
KLB
0.925 0.120 4 39420199 intron variant G/T snv 0.28 2
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs139271658
PTPRD
1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02 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
rs2710833
DDX60L ; LOC107986198
0.925 0.080 4 168488807 intron variant T/A;C snv 2
rs2980888 1.000 0.040 8 125495066 intron variant T/C snv 0.76 2
rs4640525
HESX1 ; APPL1
0.925 0.080 3 57229366 intron variant G/C snv 0.36 2
rs6006473
PARVB ; SAMM50
0.925 0.040 22 43997195 intron variant C/T snv 0.47 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
rs7674434
KLB
0.925 0.120 4 39417789 intron variant T/G snv 0.32 2
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
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
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
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
rs1492100
AGTR1
1.000 0.040 3 148719640 intron variant T/A snv 0.34 1
rs1800804
MTTP
1.000 0.040 4 99574660 intron variant T/C snv 0.26 1
rs1858999
GATAD2A
1.000 0.040 19 19386860 intron variant C/G snv 0.56 1