Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2383204
CDKN2B-AS1
0.827 0.160 9 22055049 intron variant A/G;T snv 6
rs283813
NECTIN2
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 6
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs704180
ABCC9
0.807 0.240 12 21841177 intron variant A/G snv 0.55 6
rs73069071
IAPP ; SLCO1A2
0.807 0.240 12 21357370 intron variant T/C snv 0.14 6
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 6
rs11792633
IL33 ; LOC107987046
0.882 0.280 9 6248035 intron variant C/T snv 0.35 5
rs12721109
APOC4 ; APOC4-APOC2
1.000 0.080 19 44943964 intron variant G/A snv 1.3E-02 5
rs1554483
CLOCK
0.882 0.160 4 55455650 intron variant C/G snv 0.33 5
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs1800977
ABCA1 ; LOC105376196
0.851 0.240 9 104928169 intron variant G/A;C snv 5
rs1977412
LOC105373166
0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs2279357
CYP11A1
0.851 0.160 15 74338282 intron variant T/C snv 0.69 5
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv 5
rs285
LPL
1.000 0.080 8 19957678 intron variant C/T snv 0.59 5
rs31563 0.851 0.160 5 135899917 intron variant C/A;T snv 5
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 5
rs4769874
ALOX5AP
0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs4836133
LOC105379158 ; LINC02240
0.925 0.160 5 124996410 intron variant C/A;G;T snv 5
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5