Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1878406
rs1878406 		0.807 0.200 4 147472512 intergenic variant C/A;G;T snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.810 0.500 1 2011 2014
dbSNP: rs11781551
rs11781551
LOC105375733
1.000 0.040 8 122395852 intergenic variant G/A snv 0.40
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs17045031
rs17045031
LOC105377142
1.000 0.040 3 66717940 intergenic variant G/A snv 0.10
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs17398575
rs17398575 		0.882 0.040 7 106769006 intron variant G/A snv 0.20
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs445925
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs4712972
rs4712972
SLC17A1 ; SLC17A4
0.882 0.160 6 25771819 intron variant A/C;G snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs6511720
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs6601530
rs6601530
PINX1
1.000 0.040 8 10813762 intron variant G/A snv 0.61
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs10276782
rs10276782 		1.000 0.040 7 24765621 regulatory region variant C/T snv 0.13
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.700 1.000 1 2011 2011
dbSNP: rs4888378
rs4888378
CFDP1
0.851 0.040 16 75298143 intron variant A/G snv 0.52
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.700 1.000 1 2012 2012
dbSNP: rs4901536
rs4901536
SAMD4A
0.925 0.080 14 54733816 intron variant T/C snv 0.67
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.700 1.000 1 2012 2012