Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs28939068
CST3
0.790 0.200 20 23635330 missense variant A/T snv 9
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs63750311
PSEN1
0.790 0.240 14 73192647 missense variant A/C snv 8
rs1394871591
ABCA1
0.827 0.200 9 104903619 missense variant G/C snv 4.8E-06 5
rs950592627
APP
0.827 0.200 21 26090015 missense variant G/C snv 7.0E-06 5
rs79524815
HDAC9
0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 4
rs63751254
PSEN1
0.851 0.160 14 73217210 missense variant A/G snv 4
rs34487851 0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28 3
rs1275544322
APP
0.882 0.160 21 25975185 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1297968881
APP
0.882 0.200 21 26112137 missense variant C/T snv 4.0E-06 3
rs1412095491
APP
0.882 0.200 21 26051053 missense variant C/G snv 4.0E-06 3
rs387906523
TTR
0.882 0.160 18 31593025 missense variant G/A;C snv 3
rs1337832380
MBP
0.925 0.120 18 76984810 missense variant C/T snv 2
rs35067331
TRAPPC12
1.000 0.120 2 3470314 intron variant C/T snv 0.27 1