Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2761016
ALAD
0.925 0.120 9 113391072 intron variant T/C snv 0.59 2
rs6442260
ATG7
0.925 0.160 3 11549277 intron variant G/A snv 0.42 2
rs750597831
ATM
1.000 0.120 11 108229230 missense variant C/T snv 8.0E-06 7.0E-06 2
rs2050462
CSF1
0.925 0.120 1 109930334 3 prime UTR variant T/A;G snv 2
rs333951
CSF1
0.925 0.120 1 109909068 upstream gene variant T/C snv 0.74 2
rs2504106
DAAM2
0.925 0.120 6 39854343 intron variant A/G snv 0.61 2
rs6937133
DAAM2
0.925 0.120 6 39832238 intron variant A/C;G snv 2
rs2291599
DKK3
0.925 0.120 11 11968352 intron variant T/C snv 0.83 0.85 2
rs7396187
DKK3
0.925 0.120 11 11967604 intron variant C/G snv 0.84 2
rs4903064
DPF3
0.925 0.120 14 72812712 intron variant T/C snv 0.23 2
rs12617313
EPAS1
0.925 0.120 2 46332637 intron variant A/G;T snv 2
rs7579899
EPAS1
0.925 0.120 2 46310465 intron variant A/G snv 0.52 2
rs9679290
EPAS1
0.925 0.120 2 46330505 intron variant G/C snv 0.41 2
rs1802074
EPDR1 ; SFRP4
0.925 0.120 7 37907501 missense variant C/T snv 0.20 0.24 2
rs4381241
FAF1
0.925 0.120 1 50441766 intron variant T/C snv 0.51 2
rs756787389
FLCN
0.925 0.120 17 17219129 missense variant C/T snv 1.2E-05 4.9E-05 2
rs1010980331
FLCN ; MPRIP
0.925 0.120 17 17215072 missense variant T/C snv 2
rs448012
FLT4
0.925 0.120 5 180619344 missense variant G/C snv 0.63 0.61 2
rs1259293
FSTL1
0.925 0.120 3 120421014 intron variant T/C snv 0.59 2
rs2499707
GRM4
0.925 0.120 6 34085889 intron variant T/A;C snv 2
rs7102764
GRM5
0.925 0.120 11 88778092 intron variant A/T snv 0.50 2
rs2243270
IL4
0.925 0.120 5 132678417 intron variant A/G;T snv 2
rs4787951
IL4R
0.925 0.120 16 27332642 intron variant T/C snv 0.29 2
rs10771279
ITPR2
0.925 0.120 12 26377610 intron variant T/A;C snv 0.40 2
rs8106822
LOC107985311
0.925 0.120 19 31373516 intron variant G/A snv 0.42 2