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: rs2303790
rs2303790
CETP
19 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.030 1.000 3 1996 2005
dbSNP: rs1063856
rs1063856
VWF
14 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 < 0.001 1 2005 2005
dbSNP: rs11542041
rs11542041
APOE
23 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2005 2005
dbSNP: rs281865545
rs281865545
PECAM1
18 0.695 0.360 17 64377836 missense variant C/G;T snv 0.010 1.000 1 2005 2005
dbSNP: rs371150372
rs371150372
CAD
3 0.882 0.040 2 27223972 missense variant G/A;T snv 2.8E-05; 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs532997003
rs532997003
ABCA1
3 0.882 0.040 9 104840464 missense variant T/C snv 2.0E-05 0.010 1.000 1 2005 2005
dbSNP: rs763172697
rs763172697
CAD
3 0.882 0.040 2 27233526 missense variant G/T snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs772132247
rs772132247
LPL
3 0.882 0.040 8 19959292 missense variant G/A snv 5.2E-05 7.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs774232279
rs774232279
LIPC
3 0.882 0.040 15 58548572 missense variant G/A;T snv 0.010 1.000 1 2005 2005
dbSNP: rs80356814
rs80356814
LMNA
15 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1041981
rs1041981
LTA ; LOC100287329
25 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 0.010 1.000 1 2006 2006
dbSNP: rs1131498
rs1131498
SELL ; C1orf112
13 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 0.010 1.000 1 2006 2006
dbSNP: rs121964962
rs121964962
CBS
5 0.827 0.200 21 43062988 missense variant C/T snv 1.6E-04 0.010 1.000 1 2006 2006
dbSNP: rs1541861
rs1541861
NOS3
2 0.925 0.040 7 151000245 intron variant C/A snv 0.70 0.010 1.000 1 2006 2006
dbSNP: rs2066714
rs2066714
ABCA1
13 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 0.010 1.000 1 2006 2006
dbSNP: rs2066718
rs2066718
ABCA1
7 0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 0.010 1.000 1 2006 2006
dbSNP: rs2075822
rs2075822
NOD1
1 1.000 0.040 7 30451144 intron variant A/G snv 0.19 0.010 1.000 1 2006 2006
dbSNP: rs28940578
rs28940578
MEFV
16 0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 0.010 1.000 1 2006 2006
dbSNP: rs28940579
rs28940579
MEFV
13 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs2907748
rs2907748
NOD1
1 1.000 0.040 7 30433407 non coding transcript exon variant C/T snv 0.20 0.010 1.000 1 2006 2006
dbSNP: rs3091244
rs3091244
CRP
17 0.724 0.280 1 159714875 upstream gene variant G/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs375752214
rs375752214
NOS3
22 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 0.010 1.000 1 2006 2006
dbSNP: rs5063
rs5063
CLCN6 ; NPPA ; NPPA-AS1
12 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 0.010 1.000 1 2006 2006
dbSNP: rs748954737
rs748954737
CRP
3 0.882 0.040 1 159713734 missense variant C/T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs749903604
rs749903604
APOB
3 0.882 0.080 2 21042450 missense variant G/A snv 8.0E-06 0.010 1.000 1 2006 2006