Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs556766
PIGO
9 35089051 3 prime UTR variant A/C snv 1.00 0.98 1
rs649964
KL
13 33061698 missense variant T/A;C snv 8.0E-06; 0.99 3
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 3
rs629001
MYBPHL
1 109296296 missense variant C/G;T snv 0.93 3
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
rs2280845
ENDOG ; SPOUT1
9 128820891 3 prime UTR variant T/A;C;G snv 5.7E-06; 0.72; 3.9E-04 1
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs10128711
SPTY2D1
11 18611437 intron variant T/C snv 0.64 0.55 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 3
rs753381
PLCG1 ; MIR6871
20 41168825 missense variant T/C snv 0.61 0.67 1
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 7
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 3
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs6413504
LDLR
19 11131239 intron variant A/G snv 0.45 0.39 3
rs6698843
CELSR2
0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44 3
rs6689614
CELSR2
1 109264477 synonymous variant G/A;C snv 0.44 3
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs5925
LDLR
0.851 0.200 19 11120205 synonymous variant T/C snv 0.42 0.37 3
rs2495477
PCSK9
1 55052794 splice region variant A/G snv 0.42 0.49 3