Source: GWASDB ×
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 1
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs6517147
LINC01548
21 33170482 intron variant A/G snv 0.23 1
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs11697871 20 61218983 regulatory region variant T/C snv 0.58 1
rs1857198 20 61211194 intergenic variant C/T snv 0.57 1
rs1891490 20 61228105 intergenic variant T/C snv 0.60 1
rs2426990 20 61212947 intergenic variant A/G snv 0.42 1
rs2866004 20 61249986 upstream gene variant G/A snv 0.58 1
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 1
rs6015934 20 61225004 intergenic variant G/A snv 0.57 1
rs6028074 20 61216915 intergenic variant C/G snv 0.58 1
rs6065074 20 61221161 intergenic variant G/A;T snv 1
rs6081741
LOC107987276 ; RIN2
20 19763697 intron variant G/A snv 0.65 1
rs6129076 20 61212595 intergenic variant C/T snv 0.55 1
rs6129077 20 61216286 intergenic variant C/A;G snv 1
rs6513566 20 61225053 intergenic variant A/C snv 0.60 1
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
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
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