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: rs174547
rs174547
FADS1 ; FADS2
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 2 2012 2016
dbSNP: rs6065904
rs6065904
PLTP
7 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.800 1.000 2 2009 2012
dbSNP: rs1059611
rs1059611
LPL
3 8 19967052 3 prime UTR variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs10889353
rs10889353
DOCK7
5 1 62652525 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11075253
rs11075253
PDXDC1 ; NTAN1
1 16 15054789 intron variant C/A snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs115136538
rs115136538
ADAMTS3
1 4 72456848 intron variant T/C snv 5.7E-03 0.800 1.000 1 2012 2012
dbSNP: rs115849089
rs115849089 		7 8 20054859 intergenic variant G/A snv 9.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs1160985
rs1160985
TOMM40
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs11644601
rs11644601
PDXDC1 ; RRN3
4 16 15078261 intron variant T/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs1167998
rs1167998
DOCK7
6 1 62465961 intron variant C/A snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs1168029
rs1168029
DOCK7
1 1 62503731 intron variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs1168041
rs1168041
DOCK7
2 1 62494579 non coding transcript exon variant T/C snv 0.61 0.700 1.000 1 2016 2016
dbSNP: rs12713956
rs12713956
APOB
4 2 21018633 intron variant A/G snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs1532085
rs1532085
ALDH1A2
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1532624
rs1532624
CETP
12 0.851 0.160 16 56971567 intron variant C/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs17111684
rs17111684
USP24
4 1 55159875 intron variant C/T snv 3.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs17249141
rs17249141
LDLR
4 19 11089332 upstream gene variant C/T snv 3.3E-03 0.700 1.000 1 2013 2013
dbSNP: rs17267292
rs17267292
GPC5 ; LOC105370315
2 13 92670893 intron variant T/C snv 0.22 0.700 1.000 1 2008 2008
dbSNP: rs17610395
rs17610395
CPT1A
1 11 68794860 missense variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs181807530
rs181807530
MINK1
1 17 4871519 intron variant C/G snv 4.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs186183604
rs186183604
RAD9A ; LOC100130987
1 11 67361262 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1864163
rs1864163
CETP
10 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs190121281
rs190121281 		1 19 19141970 upstream gene variant G/A snv 3.5E-03 0.700 1.000 1 2016 2016
dbSNP: rs2575876
rs2575876
ABCA1
7 9 104903458 intron variant G/A snv 0.24 0.800 1.000 1 2012 2012
dbSNP: rs312985
rs312985 		2 2 21155933 regulatory region variant A/G snv 0.75 0.700 1.000 1 2009 2009