Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2294918
PNPLA3
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs626283
TMC4 ; MBOAT7 ; LOC112268246
0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs1057972
IL15
0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7
rs2854116
APOC3
0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs2862954
ERLIN1
0.925 0.040 10 100152307 missense variant T/C snv 0.34 0.32 2
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13