Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63750512
MAPT
0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 6
rs63750301
PSEN1
0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 6
rs63749877
GRN
0.882 0.120 17 44351139 frameshift variant CACT/- delins 3
rs157590
TOMM40
0.882 0.160 19 44895459 intron variant A/C snv 0.60 3
rs63751085
GRN
0.925 0.120 17 44350767 frameshift variant CA/- del 2
rs1064725
APOC1
1.000 0.120 19 44919304 3 prime UTR variant T/G snv 3.4E-02 1
rs764232836
GRN
1.000 0.120 17 44349713 missense variant A/G snv 4.0E-06 1