Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 14
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 12
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs2585428
CYP24A1
0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs1380576
MDM4
0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 10
rs7726159
TERT
0.790 0.160 5 1282204 intron variant C/A snv 0.29 10
rs822395
ADIPOQ
0.776 0.240 3 186849018 intron variant C/A;G snv 10
rs10486567
JAZF1
0.851 0.120 7 27936944 intron variant G/A snv 0.28 9
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 9
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs17021918
PDLIM5
0.776 0.240 4 94641726 intron variant C/T snv 0.30 8
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs2011077
FGFR4
0.807 0.080 5 177094455 intron variant C/T snv 0.19 8
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8