Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 23
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 15
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;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
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 12
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 11
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 9
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
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
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 8
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 8
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 8