Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs879254850
MIR6886 ; LDLR
0.776 0.160 19 11113365 missense variant A/G;T snv 4.0E-06 9
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8
rs879254925
MIR6886 ; LDLR
0.790 0.120 19 11113680 missense variant G/T snv 8
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs5351
EDNRB-AS1 ; EDNRB
0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7
rs879254693
LDLR
0.807 0.160 19 11107424 missense variant T/A;C;G snv 7
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs1264352930
APOA1 ; APOA1-AS
0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs569033466
CETP
0.882 0.160 16 56961929 5 prime UTR variant G/A;C;T snv 4.8E-05; 2.4E-05 6
rs759003763
MIR6886 ; LDLR
0.827 0.120 19 11113585 missense variant G/A snv 6
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs1249040838
MIR6886 ; LDLR
0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 5
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs2298566
SNX19
0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5