Disease: Alzheimer's Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs283813
NECTIN2
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 3
rs11673139
NECTIN2
1.000 0.080 19 44879780 intron variant A/T snv 8.8E-02 2