Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs970866
B4GALT6
0.851 0.160 18 31681955 intron variant C/T snv 0.89 4
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 5
rs946880677
FAP
0.882 0.080 2 162224488 missense variant T/C snv 4
rs933476040
TTR
0.925 0.120 18 31595130 missense variant G/A snv 2
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs920832709
GSN
0.851 0.200 9 121321384 synonymous variant G/T snv 4
rs80356710
PRNP
0.925 0.040 20 4699655 stop gained T/G snv 3
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9
rs7982
CLU
1.000 0.040 8 27604964 missense variant A/C;G snv 0.64 0.60 1
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs767006697
MEFV
0.925 0.080 16 3254658 frameshift variant C/- delins 2
rs766474822
VEGFA
0.925 0.080 6 43770990 missense variant G/A snv 1.4E-05 2.1E-05 2
rs763852444
APP
0.882 0.120 21 26112127 missense variant G/C snv 4.0E-06 3
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs759304648
GSN
0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 9
rs745826707
RBM45
0.851 0.200 2 178112712 missense variant G/A;T snv 8.0E-06; 4.0E-06 5
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs73956431
B4GALT6
0.827 0.120 18 31699870 regulatory region variant C/T snv 8.4E-02 6
rs73069071
IAPP ; SLCO1A2
0.807 0.240 12 21357370 intron variant T/C snv 0.14 6
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23