Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs951599607
PPARG
0.925 0.040 3 12434028 missense variant G/A snv 4
rs926633
PNPLA3
1.000 22 43941653 intron variant G/A snv 0.20 1
rs903361
ADORA1
0.882 0.160 1 203122146 intron variant G/A;C snv 4
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs7946
PEMT
0.851 0.160 17 17506246 missense variant C/T snv 0.59 0.59 6
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7643645
NR1I2
0.882 0.080 3 119806650 intron variant A/G snv 0.31 3
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 10
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs72563732
ADIPOQ-AS1 ; ADIPOQ
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 5
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs6006602
SAMM50
1.000 22 43987520 non coding transcript exon variant C/T snv 0.48 1
rs6006473
PARVB ; SAMM50
0.925 0.040 22 43997195 intron variant C/T snv 0.47 2
rs6006469
SAMM50
1.000 22 43987737 non coding transcript exon variant C/G snv 0.49 1
rs6006468
SAMM50
1.000 22 43987552 non coding transcript exon variant G/C snv 0.48 1
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4823182
SAMM50
0.925 0.080 22 43981562 intron variant A/G snv 0.46 2