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
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs386833981
FBXL3 ; CLN5
0.925 0.120 13 77000517 missense variant T/G snv 3
rs7700443 5 85876294 intergenic variant T/G snv 0.57 1
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs146170087
C19orf12
0.925 0.040 19 29702747 missense variant T/C snv 2.3E-03 1.1E-03 7
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs747105516
PSPH
0.851 0.120 7 56015139 missense variant T/C snv 4.0E-06 5
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs3875089
AQP4 ; AQP4-AS1
0.925 0.080 18 26865469 intron variant T/C snv 0.19 3
rs2283368
KL
1.000 0.040 13 33019132 intron variant T/C snv 0.15 2
rs10073892
SLCO6A1
5 102391066 non coding transcript exon variant T/C snv 0.24 0.21 1
rs10512015
ANXA1
9 73166330 intron variant T/C snv 9.9E-02 1
rs73643144
TEK
9 27126454 intron variant T/C snv 3.5E-02 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs139650807
LRP10
0.925 0.080 14 22875867 missense variant T/A;C snv 6.0E-05 3