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
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 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
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 5
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs387976
NECTIN2
1.000 0.080 19 44875803 intron variant A/C;T snv 4
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs4803763
NECTIN2
1.000 0.080 19 44854034 intron variant G/A;C snv 4