Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1448674651
TYMS ; ENOSF1
0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
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
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 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
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
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
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs1424266770
CASP3
0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 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