Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs4772201
LOC107984558
1.000 0.080 13 99434005 upstream gene variant A/G snv 0.22 1
rs727263
UBAC2 ; FKSG29
1.000 0.080 13 99351854 intron variant G/A;T snv 0.17; 7.9E-06 1
rs7809799
KPNA7
0.925 0.120 7 99162881 regulatory region variant G/A;T snv 2
rs16914086
TBC1D2
1.000 0.080 9 98226195 intron variant G/A snv 9.8E-02 1
rs4900384 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 4
rs391745 0.925 0.080 X 97839482 intergenic variant C/G;T snv 3
rs4763879
CD69
0.925 0.160 12 9757568 intron variant G/A snv 0.28 2
rs9320598
LOC101927314
1.000 0.080 6 97571204 intron variant A/G snv 0.15 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11052877
CD69
1.000 0.080 12 9753094 3 prime UTR variant A/G snv 0.34 1
rs10466829
CLECL1
1.000 0.080 12 9723495 intron variant G/A snv 0.55 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs4763655
KLRB1 ; LOC107987174
1.000 0.080 12 9602982 intron variant G/A snv 0.32 1
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs532834 1.000 0.080 1 93002505 intergenic variant A/G;T snv 1
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs9523787
GPC5-AS1 ; GPC5
1.000 0.080 13 92711507 intron variant G/T snv 0.15 1
rs6680578
EVI5
1.000 0.080 1 92711321 intron variant T/A snv 0.57 1
rs11810217
EVI5
1.000 0.080 1 92682820 intron variant C/T snv 0.20 1
rs9523762
LOC105370315 ; GPC5
0.925 0.120 13 92679633 intron variant G/A snv 0.39 2
rs10735781
EVI5
1.000 0.080 1 92655550 intron variant G/C snv 0.57 1