Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2277844
PLA2G6
22 38181508 intron variant G/A snv 0.53 2
rs4821816
GTPBP1
22 38717129 intron variant G/A snv 0.37 1
rs6001193 22 38678732 intron variant A/G;T snv 1
rs9611441 22 40943363 regulatory region variant G/A;C snv 1
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 5
rs4817984 1.000 0.080 21 39093140 intergenic variant C/A;G snv 2
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 3
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs3762220 20 18797336 upstream gene variant G/A;T snv 2
rs117246187
RIPOR3
20 50690397 intron variant A/G snv 5.7E-02 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 8
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 5
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 4
rs1529711
CARM1
1.000 0.080 19 10912758 intron variant C/T snv 0.13 3
rs157595 1.000 0.080 19 44922203 upstream gene variant A/G;T snv 3
rs1688043
HPN-AS1 ; HPN
19 35062437 intron variant C/G;T snv 3
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 3