Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1251713297
PRMT7
0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs779021719
HAMP
0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 5
rs879254597
LDLR
0.851 0.120 19 11105528 stop gained G/A;T snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614