Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs2281292
SAMM50 ; PARVB
1.000 22 43999509 intron variant A/C snv 0.44 0.47 1
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs2228530
PPP1CB
1.000 2 28778825 missense variant A/C;G snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 5
rs2072906
PNPLA3
0.851 0.160 22 43937292 intron variant A/G snv 0.25 0.20 4
rs7643645
NR1I2
0.882 0.080 3 119806650 intron variant A/G snv 0.31 3
rs3761472
SAMM50
0.925 0.040 22 43972242 missense variant A/G snv 0.21 0.18 2
rs4823182
SAMM50
0.925 0.080 22 43981562 intron variant A/G snv 0.46 2
rs1010022
PNPLA3
1.000 22 43940430 intron variant A/G snv 0.20 1
rs2073079
SAMM50
1.000 22 43989714 intron variant A/G snv 0.21 1
rs3788604
SAMM50
1.000 22 43992537 intron variant A/G snv 0.48 1
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4674344
CYP27A1
1.000 2 218805152 intron variant A/T snv 0.53 1
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs12597002
CETP
1.000 16 56968492 intron variant C/A snv 0.25 3
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs2076211
PNPLA3
1.000 22 43933198 intron variant C/A;T snv 0.18 3
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs2072907
PNPLA3
0.882 0.120 22 43936773 intron variant C/G snv 0.20 3