Source: GWASCAT

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: rs17114046
rs17114046
0.925 0.040 1 56500678 intron variant A/G snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2011
dbSNP: rs10755578
rs10755578
LPA
0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2009 2009
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: rs11057830
rs11057830
0.851 0.040 12 124822507 intron variant G/A snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2017 2019
dbSNP: rs11638352
rs11638352
0.925 0.040 15 44000939 intron variant C/A;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs11915606
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
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: rs12290663
rs12290663
0.925 0.040 11 26141193 intergenic variant G/A snv 5.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
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: 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: rs12524865
rs12524865
1.000 0.040 6 133875536 intron variant C/A snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2012
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: 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
dbSNP: rs13279522
rs13279522
1.000 0.040 8 66062017 intron variant T/C snv 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2012 2012
dbSNP: rs1332844
rs1332844
1.000 0.040 6 12888772 intron variant C/T snv 0.61
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs138741635
rs138741635
0.925 0.040 3 60942161 intron variant T/A;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs1395821
rs1395821
1.000 0.040 4 147126398 intron variant C/T snv 0.70
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs144610116
rs144610116
0.925 0.040 4 38941227 intron variant T/C snv 8.6E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs144972973
rs144972973
0.925 0.040 15 44272494 intergenic variant A/G snv 1.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs145044782
rs145044782
0.925 0.040 7 7995866 intron variant G/A snv 2.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs147204125
rs147204125
0.925 0.040 14 73609035 intron variant A/G snv 9.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs147233090
rs147233090
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs148121703
rs148121703
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs149232047
rs149232047
0.925 0.040 6 126276990 intergenic variant A/G snv 1.5E-04
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs151269874
rs151269874
0.925 0.040 16 75549741 intron variant C/T snv 6.2E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017