Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 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
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 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
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12