Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1427575965
C2orf42 ; TIA1
0.925 0.120 2 70212796 missense variant G/A snv 8.0E-06 3
rs267606663
APOE
0.925 0.080 19 44909021 missense variant G/A;C snv 7.3E-06 3
rs3763040
AQP4 ; AQP4-AS1
0.925 0.080 18 26864410 intron variant G/A;T snv 3
rs3763043
AQP4 ; AQP4-AS1
0.925 0.080 18 26855854 3 prime UTR variant C/T snv 0.30 3
rs386833981
FBXL3 ; CLN5
0.925 0.120 13 77000517 missense variant T/G snv 3
rs3875089
AQP4 ; AQP4-AS1
0.925 0.080 18 26865469 intron variant T/C snv 0.19 3
rs55781031
BCHE
0.925 0.080 3 165786432 intron variant A/G snv 5.3E-02 3
rs62256378
SUCLG2
0.925 0.080 3 67406609 intron variant G/A;C snv 3
rs6910730
TREM1
0.925 0.080 6 41278895 intron variant A/G snv 0.21 3
rs796052957
SCN1A-AS1 ; SCN1A
0.925 0.040 2 166054735 missense variant A/G snv 3
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs515726205
C19orf12
0.882 0.040 19 29702966 missense variant C/T snv 2.4E-05 1.4E-05 7
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 6
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs765061840
SPG11
0.882 0.120 15 44633619 stop gained G/A snv 1.2E-05 7.0E-06 6
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs371334506
SPG11
0.882 0.120 15 44565954 missense variant A/C;G snv 4.0E-06 5
rs9951307
AQP4-AS1
0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs112422930
MUTYH
0.882 0.160 1 45332409 missense variant A/C snv 7.0E-06 4
rs1143684
NQO2
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84 4
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21