Source: CURATED

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 12
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
rs289714
CETP
16 56973539 intron variant G/A snv 0.76; 4.0E-06 0.70 5
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
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 9
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 73
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 64
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 3
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 3
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 2
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 9