Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3827385
SAMM50
1.000 22 43992937 intron variant T/C snv 0.21 1
rs4674344
CYP27A1
1.000 2 218805152 intron variant A/T snv 0.53 1
rs4823179
PNPLA3
1.000 22 43945313 intron variant T/C snv 0.20 1
rs6006468
SAMM50
1.000 22 43987552 non coding transcript exon variant G/C snv 0.48 1
rs6006469
SAMM50
1.000 22 43987737 non coding transcript exon variant C/G snv 0.49 1
rs6006602
SAMM50
1.000 22 43987520 non coding transcript exon variant C/T snv 0.48 1
rs926633
PNPLA3
1.000 22 43941653 intron variant G/A snv 0.20 1
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 5
rs951599607
PPARG
0.925 0.040 3 12434028 missense variant G/A snv 4
rs2235776
SAMM50
0.925 0.040 22 43982119 intron variant C/T snv 0.24 3
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs72563732
ADIPOQ-AS1 ; ADIPOQ
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs2073080
PARVB ; SAMM50
0.925 0.040 22 43998522 intron variant C/T snv 0.20 2
rs3761472
SAMM50
0.925 0.040 22 43972242 missense variant A/G snv 0.21 0.18 2
rs6006473
PARVB ; SAMM50
0.925 0.040 22 43997195 intron variant C/T snv 0.47 2
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs7643645
NR1I2
0.882 0.080 3 119806650 intron variant A/G snv 0.31 3
rs4823182
SAMM50
0.925 0.080 22 43981562 intron variant A/G snv 0.46 2
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 10
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 6