Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2954029
rs2954029 		14 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 8 2010 2019
dbSNP: rs6511720
rs6511720
LDLR
15 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.800 1.000 7 2010 2019
dbSNP: rs10401969
rs10401969
SUGP1
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.800 1.000 6 2010 2018
dbSNP: rs2000999
rs2000999
HPR ; TXNL4B
7 1.000 0.080 16 72074194 intron variant G/A snv 0.16 0.800 1.000 6 2010 2018
dbSNP: rs12670798
rs12670798
DNAH11 ; LOC105375183
5 1.000 0.040 7 21567734 intron variant T/C snv 0.26 0.800 1.000 5 2009 2018
dbSNP: rs1532085
rs1532085
ALDH1A2
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.800 1.000 5 2009 2018
dbSNP: rs1883025
rs1883025
ABCA1
13 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.800 1.000 5 2010 2018
dbSNP: rs4299376
rs4299376
ABCG8 ; LOC102725159
11 0.851 0.120 2 43845437 intron variant G/C;T snv 0.800 1.000 5 2010 2019
dbSNP: rs10038095
rs10038095
HMGCR
3 5 75341886 intron variant A/T snv 0.38 0.800 1.000 4 2012 2019
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.800 1.000 4 2012 2019
dbSNP: rs10889353
rs10889353
DOCK7
5 1 62652525 intron variant A/C;T snv 0.800 1.000 4 2009 2019
dbSNP: rs11207995
rs11207995
DOCK7
4 1 62583880 intron variant A/C;G snv 0.800 1.000 4 2013 2019
dbSNP: rs11220462
rs11220462
ST3GAL4
3 11 126374057 intron variant G/A snv 0.12 0.800 1.000 4 2010 2018
dbSNP: rs1564348
rs1564348
SLC22A1
3 6 160157828 intron variant T/C snv 0.14 0.800 1.000 4 2010 2019
dbSNP: rs1800588
rs1800588
LIPC ; ALDH1A2
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 4 2012 2018
dbSNP: rs2131925
rs2131925
DOCK7
6 1 62560271 intron variant G/T snv 0.57 0.800 1.000 4 2010 2019
dbSNP: rs2238675
rs2238675
NCAN
4 19 19225799 intron variant C/T snv 9.4E-02 0.800 1.000 4 2012 2019
dbSNP: rs2255141
rs2255141
GPAM
5 10 112174128 intron variant A/G;T snv 0.800 1.000 4 2010 2019
dbSNP: rs2575876
rs2575876
ABCA1
7 9 104903458 intron variant G/A snv 0.24 0.800 1.000 4 2012 2018
dbSNP: rs507666
rs507666
ABO
8 1.000 0.040 9 133273983 intron variant A/G snv 0.800 1.000 4 2013 2019
dbSNP: rs7206971
rs7206971
EFCAB13
3 17 47347749 intron variant G/A;T snv 0.47 0.800 1.000 4 2010 2018
dbSNP: rs7499892
rs7499892
CETP
7 16 56972678 intron variant C/G;T snv 0.800 1.000 4 2012 2019
dbSNP: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.800 1.000 4 2012 2019
dbSNP: rs780094
rs780094
GCKR
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.800 1.000 4 2012 2019
dbSNP: rs10128711
rs10128711
SPTY2D1
2 11 18611437 intron variant T/C snv 0.64 0.55 0.800 1.000 3 2010 2018