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: rs405509
rs405509
APOE
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.700 1.000 3 2012 2013
dbSNP: rs4803750
rs4803750
BCL3
22 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 0.700 1.000 3 2008 2013
dbSNP: rs515135
rs515135 		9 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 0.700 1.000 3 2009 2013
dbSNP: rs602633
rs602633 		10 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 0.700 1.000 3 2008 2012
dbSNP: rs660240
rs660240
CELSR2
6 1 109275216 3 prime UTR variant T/C snv 0.75 0.700 1.000 3 2008 2012
dbSNP: rs7412
rs7412
APOE
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 3 2012 2013
dbSNP: rs10402271
rs10402271 		7 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 0.700 1.000 2 2008 2012
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 2 2012 2012
dbSNP: rs11065987
rs11065987 		17 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 0.700 1.000 2 2010 2013
dbSNP: rs11136341
rs11136341
PLEC
3 8 143969375 intron variant A/G snv 0.40 0.700 1.000 2 2010 2013
dbSNP: rs11220462
rs11220462
ST3GAL4
3 11 126374057 intron variant G/A snv 0.12 0.700 1.000 2 2010 2013
dbSNP: rs11668477
rs11668477 		7 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 0.700 1.000 2 2008 2009
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
21 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 0.700 1.000 2 2010 2013
dbSNP: rs11806638
rs11806638
PCSK9
3 1 55052487 intron variant C/A;G snv 0.700 1.000 2 2012 2012
dbSNP: rs12027135
rs12027135
MACO1
3 1 25449242 intron variant A/T snv 0.50 0.700 1.000 2 2010 2013
dbSNP: rs12654264
rs12654264
HMGCR
7 0.925 0.120 5 75352778 intron variant A/T snv 0.38 0.700 1.000 2 2008 2012
dbSNP: rs12713956
rs12713956
APOB
4 2 21018633 intron variant A/G snv 0.14 0.700 1.000 2 2012 2013
dbSNP: rs12721046
rs12721046
APOC1
8 19 44917997 intron variant G/A snv 0.11 0.700 1.000 2 2012 2012
dbSNP: rs12721109
rs12721109
APOC4 ; APOC4-APOC2
5 1.000 0.080 19 44943964 intron variant G/A snv 1.3E-02 0.700 1.000 2 2012 2012
dbSNP: rs1564348
rs1564348
SLC22A1
3 6 160157828 intron variant T/C snv 0.14 0.700 1.000 2 2010 2013
dbSNP: rs16996148
rs16996148 		8 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 0.700 1.000 2 2008 2012
dbSNP: rs17242787
rs17242787
LDLR
3 19 11091784 intron variant T/A snv 6.4E-03 0.700 1.000 2 2012 2012
dbSNP: rs17248720
rs17248720
LDLR
4 19 11087511 upstream gene variant C/T snv 0.16 0.700 1.000 2 2012 2012
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.700 1.000 2 2010 2013
dbSNP: rs2072183
rs2072183
NPC1L1
6 0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 0.700 1.000 2 2010 2013