Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 2
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs6557781
DMTN
8 22080156 intron variant T/A;C snv 0.84 2
rs2738464
SPC24 ; LDLR
1.000 0.120 19 11131631 3 prime UTR variant G/C snv 0.82 0.80 2
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs278981
RBM47
4 40425993 missense variant T/C snv 0.75 0.74 1
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67 3
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs10128711
SPTY2D1
11 18611437 intron variant T/C snv 0.64 0.55 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 1
rs2183573
BRWD1
21 39202379 missense variant A/G snv 0.63 0.61 2
rs753381
PLCG1 ; MIR6871
20 41168825 missense variant T/C snv 0.61 0.67 2
rs1126627
HEATR1
1 236555320 missense variant T/C snv 0.61 0.60 1
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 1
rs871841
ARHGEF15
17 8313150 missense variant T/C snv 0.56 0.58 2
rs2270445
ARHGEF15
17 8316160 intron variant A/G snv 0.55 0.58 1
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 2
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 1
rs2274159
WHRN
9 114403966 missense variant A/G snv 0.48 0.41 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs721772
RPAP1
15 41537032 synonymous variant A/G snv 0.48 0.42 4
rs2495477
PCSK9
1 55052794 splice region variant A/G snv 0.42 0.49 2