Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6
rs6558172
BIN3
8 22634539 intron variant G/A;C snv 0.70; 7.8E-06 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs2293889
TRPS1
8 115586972 intron variant T/C;G snv 2.0E-04; 0.65 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1877031
STARD3
0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52 1
rs2013208
RBM5 ; RBM6
3 50091966 intron variant C/T snv 0.61 0.56 3
rs326214
MADD
11 47276809 synonymous variant G/A snv 0.59 0.56 1
rs2494748
AKT1
14 104792555 intron variant C/T snv 0.51 0.48 2
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs2058804
KCTD10
12 109471206 missense variant A/C;G snv 0.50 1
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 2
rs4783961
CETP
0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 1
rs235314
PTTG1IP
21 44851537 missense variant C/T snv 0.48 0.46 3
rs721772
RPAP1
15 41537032 synonymous variant A/G snv 0.48 0.42 4
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 4
rs10948059
CNPY3-GNMT ; GNMT
0.925 0.080 6 42960723 upstream gene variant C/G;T snv 0.39 1
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs11553746
ACP1
1.000 0.080 2 272203 missense variant C/T snv 0.31 0.28 1