Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13