Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2498786
AKT1
0.925 0.160 14 104796031 upstream gene variant C/G snv 0.50 2
rs7907690
SORCS1
0.925 0.160 10 107102369 intron variant A/G snv 0.60 2
rs1544210 0.882 0.240 10 92728044 regulatory region variant G/A snv 0.39 3
rs163182
KCNQ1
0.882 0.160 11 2822986 intron variant G/A;C snv 3
rs2251101
IDE
0.882 0.160 10 92451547 downstream gene variant C/A;T snv 3
rs4646953
IDE
0.882 0.160 10 92574198 upstream gene variant A/G snv 0.17 3
rs16847897
LRRC31
0.851 0.320 3 169850328 intron variant G/A;C snv 4
rs17747324
TCF7L2
0.925 0.160 10 112992744 intron variant T/C snv 0.17 4
rs2070424
SOD1
0.851 0.200 21 31667007 non coding transcript exon variant A/G snv 0.13 4
rs2209972
MARK2P9
0.851 0.240 10 92419271 non coding transcript exon variant C/T snv 0.32 4
rs223330
CISD2
0.851 0.160 4 102872502 intron variant T/A;C snv 4
rs391300
SRR
0.882 0.160 17 2312964 intron variant T/C snv 0.58 4
rs890293
CYP2J2
0.851 0.200 1 59926822 upstream gene variant C/A snv 8.6E-02 4
rs1800977
ABCA1 ; LOC105376196
0.851 0.240 9 104928169 intron variant G/A;C snv 5
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs7755
CD36
0.882 0.200 7 80676955 3 prime UTR variant G/A snv 0.37 5
rs784567
TARBP2 ; MAP3K12
0.851 0.320 12 53500681 non coding transcript exon variant G/A;T snv 5
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs754203
CYP46A1
0.807 0.200 14 99691630 non coding transcript exon variant A/G snv 0.27 6
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
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8