Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2338796
FBXL20
17 39399374 intron variant A/G snv 0.27 1
rs3805382
NMU
4 55605384 intron variant A/G snv 0.36 0.29 1
rs7670121
NR3C2
4 148207444 intron variant A/G snv 0.24 1
rs838142
FUT1 ; IZUMO1
19 48748894 3 prime UTR variant A/G snv 0.39 1
rs1124694
LINC02752
11 11077129 intron variant A/G;T snv 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs185291443 2 226120788 intergenic variant C/A;G snv 1
rs13394343 2 85527219 intergenic variant C/A;T snv 1
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs10995311
ADO
10 62805174 missense variant C/G snv 0.35 0.31 3
rs11162351
AK5
1 77479047 intron variant C/G snv 0.31 1
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs2470893
CYP1A1
0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 8
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2
rs10157710 1 47496019 downstream gene variant C/T snv 0.78 1
rs12727980
LINC00862
1 200289967 intron variant C/T snv 0.54 1
rs1276720
CUBN
10 16929427 intron variant C/T snv 0.65 1
rs144994089
AQP7
9 33385158 missense variant C/T snv 7.0E-04 8.2E-04 1
rs183131780
LOC105373914 ; LOC107985992
2 225820170 intergenic variant C/T snv 1.0E-03 1
rs189107782
FRG1-DT
4 189807855 intron variant C/T snv 1.5E-03 1
rs2601006
CCT2 ; MIR3913-1
12 69585737 5 prime UTR variant C/T snv 0.39 1
rs35311980 2 228295484 intergenic variant C/T snv 4.9E-05 1
rs6768627
MYL3
3 46853886 intron variant C/T snv 0.13 1
rs702634
ARL15
1.000 0.080 5 53975590 intron variant G/A snv 0.72 3
rs17158386 7 29765745 regulatory region variant G/A snv 0.19 2