Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs4645978
CASP9 ; DNAJC16
0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 7
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 7
rs12108497
PRIMPOL ; CASP3
0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs12587742
DCAF4
0.851 0.080 14 72926683 intron variant G/A snv 0.18 5