Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs8191664
NEIL2
0.807 0.200 8 11786044 missense variant G/A;C;T snv 4.0E-05; 3.8E-02 7
rs121912456
SOD1 ; LOC102724449
0.851 0.120 21 31659806 missense variant G/C snv 6
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs63750301
PSEN1
0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 6
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
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
rs544706237
REG1A
0.851 0.120 2 79121649 missense variant A/G;T snv 8.0E-06; 5.2E-05 5
rs747105516
PSPH
0.851 0.120 7 56015139 missense variant T/C snv 4.0E-06 5
rs1557136818
MECP2
0.925 0.120 X 154031259 missense variant C/T snv 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs63751011
MAPT
0.925 0.120 17 46010418 intron variant C/T snv 4
rs1372439127
GRN
0.925 0.080 17 44352420 missense variant A/G snv 4.0E-06 3
rs139650807
LRP10
0.925 0.080 14 22875867 missense variant T/A;C snv 6.0E-05 3
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
rs386833981
FBXL3 ; CLN5
0.925 0.120 13 77000517 missense variant T/G snv 3
rs62256378
SUCLG2
0.925 0.080 3 67406609 intron variant G/A;C snv 3
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs796052957
SCN1A-AS1 ; SCN1A
0.925 0.040 2 166054735 missense variant A/G snv 3
rs1554950703
LOC105378526 ; HTRA1
1.000 0.200 10 122489463 missense variant C/G snv 2