Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17