Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11668327
TOMM40
1.000 0.080 19 44895376 intron variant G/C snv 0.12 2
rs11673139
NECTIN2
1.000 0.080 19 44879780 intron variant A/T snv 8.8E-02 2
rs117905930 1.000 0.080 9 88973603 intron variant C/A;T snv 2
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs12148780
ALDH1A2
1.000 0.080 15 58289090 intron variant A/G snv 0.14 2
rs12285364
SORL1
1.000 0.080 11 121522517 intron variant C/T snv 6.7E-02 2
rs1256059
ESR2
1.000 0.080 14 64243699 intron variant A/G;T snv 2
rs12610605
NECTIN2
1.000 0.080 19 44867581 intron variant G/A snv 0.15 2
rs12805422 1.000 0.080 11 45818338 intron variant G/A snv 0.42 2
rs1287723181
APP
1.000 0.080 21 25954680 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs141622900 1.000 0.080 19 44923535 upstream gene variant G/A snv 5.9E-02 2
rs1470272477
TBK1
1.000 0.080 12 64495561 missense variant G/C snv 2
rs147906088 1.000 0.080 7 54496119 intergenic variant C/A;T snv 2
rs1481950
ATP6V1H
1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs148933445
CBLC
1.000 0.080 19 44799247 intron variant G/A snv 1.2E-02 2
rs1582763
MS4A4A
1.000 0.080 11 60254475 intron variant G/A snv 0.28 2
rs1871047
NECTIN2
1.000 0.080 19 44848489 intron variant A/G snv 0.31 2
rs1925458
LOC102724749 ; LOC105374976
1.000 0.080 6 23378723 intron variant G/T snv 0.14 2
rs1936246
LOC101927293
1.000 0.080 6 58045670 intron variant T/C;G snv 2
rs200396597
APP
1.000 0.080 21 25881743 missense variant C/T snv 7.0E-06 2
rs201792381
APP
1.000 0.080 21 25997384 missense variant G/A;C snv 1.6E-05 2
rs202218688
APP
1.000 0.080 21 26000131 missense variant C/A;T snv 4.0E-06; 5.6E-05 2
rs2278317
RYR3
1.000 0.080 15 33768539 intron variant C/T snv 0.67 2
rs2422493
ABCA1 ; LOC105376196
1.000 0.080 9 104928714 intron variant G/A snv 0.48 2
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2