Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2279590
CLU
0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69 5
rs4151667 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs28936379 0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs3734254 0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 14
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63