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: rs10757274
rs10757274
0.701 0.320 9 22096056 intron variant A/G snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 1 2008 2016
dbSNP: rs671
rs671
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 1 2010 2020
dbSNP: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2011 2018
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2011 2019
dbSNP: rs12190287
rs12190287
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2017
dbSNP: rs3184504
rs3184504
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2018
dbSNP: rs4420638
rs4420638
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2009 2016
dbSNP: rs7865618
rs7865618
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2016
dbSNP: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2018
dbSNP: rs3869109
rs3869109
0.851 0.160 6 31216419 intergenic variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2012 2013
dbSNP: rs562338
rs562338
0.807 0.160 2 21065449 intergenic variant A/G snv 0.69
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2010 2016
dbSNP: rs974819
rs974819
0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2012
dbSNP: rs10401969
rs10401969
0.776 0.240 19 19296909 intron variant T/C snv 0.10
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2016
dbSNP: rs10953541
rs10953541
1.000 0.040 7 107604100 intron variant C/T snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs11066015
rs11066015
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2013 2013
dbSNP: rs11752643
rs11752643
0.925 0.120 6 32701596 downstream gene variant C/T snv 2.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2012 2012
dbSNP: rs12200560
rs12200560
1.000 0.040 6 96632322 intergenic variant A/G snv 0.36
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2012 2012
dbSNP: rs1231206
rs1231206
1.000 0.040 17 2222311 intron variant G/A snv 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
dbSNP: rs12449964
rs12449964
1.000 0.040 17 17641390 regulatory region variant C/T snv 0.36
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
dbSNP: rs12734338
rs12734338
0.925 0.120 1 202500595 intron variant T/C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2013 2013
dbSNP: rs12936587
rs12936587
0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
dbSNP: rs13232179
rs13232179
1.000 0.040 7 151423862 upstream gene variant T/A;C snv 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011