Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10524523
TOMM40
0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 7
rs747604554
FANCD2
1.000 0.080 3 10065441 frameshift variant TT/- delins 4.0E-06 1
rs281865161
APP
0.925 0.080 21 25897626 missense variant TC/GA mnv 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs1800866
SIGMAR1
0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 8
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs63750050
PSEN1
0.925 0.080 14 73198106 missense variant T/G snv 5
rs2070045
SORL1
0.851 0.080 11 121577381 synonymous variant T/G snv 0.32 0.23 4
rs79524815
HDAC9
0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 4
rs1291370551
GRN
0.882 0.120 17 44349468 missense variant T/G snv 4.0E-06 3
rs3211956
CD36
0.925 0.160 7 80674446 intron variant T/G snv 6.7E-02 3
rs63749961
PSEN1
0.925 0.080 14 73192772 missense variant T/G snv 3
rs10426401
LOC107985305 ; PVR
1.000 0.080 19 44644419 intron variant T/G snv 0.32 2
rs2147363
ATP7B
0.925 0.200 13 51968660 intron variant T/G snv 0.69 2
rs56214552
TRIQK
1.000 0.080 8 93011994 intron variant T/G snv 0.24 2