Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
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
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 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
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10