Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs2276466
ERCC4
0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv 15
rs34330
CDKN1B ; GPR19
0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 15
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs3811463
LIN28A
0.752 0.400 1 26427451 3 prime UTR variant T/A;C snv 14
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs3810366
ERCC2
0.732 0.280 19 45370684 5 prime UTR variant G/C;T snv 12
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs121912431
SOD1
0.742 0.160 21 31663829 missense variant G/A;C snv 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs391957
HSPA5 ; LOC107987127
0.763 0.240 9 125241745 non coding transcript exon variant T/C snv 0.72 10
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs35870237
LRRK2
0.763 0.120 12 40340404 missense variant T/C snv 9
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 9
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9
rs8173
AURKA
0.763 0.240 20 56369735 3 prime UTR variant C/G;T snv 9
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 8
rs1501899
CASR
0.790 0.240 3 122188481 intron variant A/G snv 0.62 8