Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 12
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 12
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 12
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 11
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 11
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 11
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 10
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 10
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 10
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 9