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
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 3
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 2
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 2
rs7700443 5 85876294 intergenic variant T/G snv 0.57 1
rs10512015
ANXA1
9 73166330 intron variant T/C snv 9.9E-02 1
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 1
rs2973488
CTNND2
5 11043805 intron variant A/T snv 0.19 1
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1