Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015909000
NFIB
1.000 0.080 9 14146790 missense variant A/G snv 1
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
rs115865530
PSEN1
0.925 0.080 14 73206449 missense variant A/G snv 1.4E-04 4.2E-05 2
rs1179768627
PSEN1
0.925 0.080 14 73198064 missense variant T/G snv 4.0E-06 2
rs1215971988
PSEN2
1.000 0.080 1 226885618 missense variant T/C snv 4.0E-06 7.0E-06 1
rs121917808
PSEN1
0.882 0.080 14 73219192 missense variant C/A snv 3
rs1220355764
APP
0.925 0.080 21 26022037 missense variant T/C snv 2
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs1281129992
APP
0.882 0.080 21 25891730 missense variant C/T snv 4.0E-06 3
rs1302192564
APP
0.925 0.080 21 26000164 missense variant G/A snv 2
rs1307925400
APP
1.000 0.080 21 26112001 missense variant C/G;T snv 4.0E-06 1
rs1347585131
APP
1.000 0.080 21 26021974 missense variant T/C snv 4.0E-06 1
rs1348800465
MAPT
1.000 0.080 17 45991491 missense variant C/G;T snv 4.0E-06; 4.0E-06 1
rs139155954
SORBS2
1.000 0.080 4 185662115 missense variant C/G;T snv 6.0E-05 1
rs1393704451
RANBP2 ; SH3RF3 ; SH3RF3-AS1
1.000 0.080 2 109129746 missense variant A/G snv 1
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs140501902
PSEN2
0.807 0.160 1 226883774 missense variant C/T snv 3.6E-03 3.4E-03 6
rs1451944248
APP
0.925 0.080 21 25975964 missense variant G/A snv 2
rs1459435816
APP
1.000 0.080 21 26053249 missense variant G/A snv 4.0E-06 1
rs1482790603
PSEN2
1.000 0.080 1 226891284 missense variant T/C snv 1.2E-05 7.0E-06 1
rs1490931437
TP53
0.925 0.120 17 7673260 missense variant G/A snv 2
rs1712572
LINC00882
1.000 0.080 3 106898231 non coding transcript exon variant A/C;G;T snv 1
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226