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: rs6511720
rs6511720
LDLR
15 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.800 1.000 17 2008 2019
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 16 2007 2019
dbSNP: rs646776
rs646776
CELSR2
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 12 2008 2019
dbSNP: rs12740374
rs12740374
CELSR2
16 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.800 1.000 11 2008 2019
dbSNP: rs12916
rs12916
HMGCR ; CERT1
12 0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 0.800 1.000 10 2010 2019
dbSNP: rs599839
rs599839
PSRC1
27 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 0.800 1.000 10 2008 2019
dbSNP: rs4299376
rs4299376
ABCG8 ; LOC102725159
11 0.851 0.120 2 43845437 intron variant G/C;T snv 0.800 1.000 9 2010 2019
dbSNP: rs562338
rs562338 		21 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 0.800 1.000 8 2008 2019
dbSNP: rs660240
rs660240
CELSR2
6 1 109275216 3 prime UTR variant T/C snv 0.75 0.800 1.000 8 2008 2019
dbSNP: rs10401969
rs10401969
SUGP1
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.800 1.000 7 2009 2018
dbSNP: rs11206510
rs11206510 		16 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 0.800 1.000 7 2008 2019
dbSNP: rs2000999
rs2000999
HPR ; TXNL4B
7 1.000 0.080 16 72074194 intron variant G/A snv 0.16 0.800 1.000 7 2010 2019
dbSNP: rs2954029
rs2954029 		14 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 7 2010 2019
dbSNP: rs515135
rs515135 		9 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 0.800 1.000 7 2009 2019
dbSNP: rs629301
rs629301
CELSR2
22 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 0.800 1.000 7 2008 2019
dbSNP: rs6882076
rs6882076
TIMD4
9 0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 0.800 1.000 7 2010 2019
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.800 1.000 6 2012 2019
dbSNP: rs174546
rs174546
FADS1 ; FADS2
17 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 0.800 1.000 6 2009 2019
dbSNP: rs2479409
rs2479409
PCSK9
4 1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 0.800 1.000 6 2010 2019
dbSNP: rs4722551
rs4722551
LOC105375199
5 7 25952206 upstream gene variant T/C;G snv 0.800 1.000 6 2013 2019
dbSNP: rs579459
rs579459 		28 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 6 2013 2019
dbSNP: rs7528419
rs7528419
CELSR2
13 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 0.800 1.000 6 2012 2019
dbSNP: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.800 1.000 6 2010 2019
dbSNP: rs9987289
rs9987289
LOC157273
10 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 0.800 1.000 6 2010 2019
dbSNP: rs1065853
rs1065853 		5 19 44909976 non coding transcript exon variant G/A;C;T snv 0.800 1.000 5 2013 2019