Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs6591182
EHBP1L1
0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs7674434
KLB
0.925 0.120 4 39417789 intron variant T/G snv 0.32 2
rs2668423
PWWP3A
1.000 0.040 19 1370527 intron variant T/G snv 0.73 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs3810622
PNPLA3
1.000 0.040 22 43942254 intron variant T/C;G snv 0.40 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs3816873
MTTP
0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs2980888 1.000 0.040 8 125495066 intron variant T/C snv 0.76 2
rs6503695
STAT3
0.925 0.040 17 42347515 intron variant T/C snv 0.33 2
rs887304
CRACR2A
0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs11166927
TRAPPC9
1.000 0.040 8 139784177 intron variant T/C snv 0.39 1
rs12373751
ERBB4
1.000 0.040 2 212072166 intron variant T/C snv 0.62 1
rs13428113
LOC107985940 ; INSIG2
1.000 0.040 2 118089309 intron variant T/C snv 0.51 1