Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs34487851 0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28 1
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 1
rs79524815
HDAC9
0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02 1
rs35067331
TRAPPC12
1.000 0.120 2 3470314 intron variant C/T snv 0.27 1