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: rs1537376
rs1537376
1.000 0.040 9 22116221 intron variant T/C snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs157580
rs157580
0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs16867808
rs16867808
1.000 0.040 6 27495905 intron variant T/C snv 6.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs16948048
rs16948048
0.925 0.040 17 49363104 intron variant A/G snv 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs16982520
rs16982520
1.000 0.040 20 59183665 intron variant A/G snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs17114036
rs17114036
0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
dbSNP: rs17321515
rs17321515
0.776 0.200 8 125474167 intron variant A/G snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.730 0.750 1 2009 2019
dbSNP: rs17367504
rs17367504
1.000 0.040 1 11802721 intron variant A/G snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs17609940
rs17609940
1.000 0.040 6 35067023 intron variant G/C snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs17772583
rs17772583
0.925 0.120 5 132617818 intron variant A/G snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1800588
rs1800588
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.720 1.000 1 2009 2013
dbSNP: rs1800609
rs1800609
1.000 0.040 9 130855797 intron variant T/C snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs1864163
rs1864163
0.882 0.120 16 56963321 intron variant G/A snv 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1883025
rs1883025
0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1918974
rs1918974
1.000 0.040 3 169448100 intron variant C/T snv 0.57
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1994016
rs1994016
0.851 0.160 15 78787892 intron variant C/T snv 0.30
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs2076890
rs2076890
1.000 0.040 6 25420516 intron variant G/T snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs2133189
rs2133189
0.925 0.040 1 222641100 intron variant C/T snv 0.56
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs2144300
rs2144300
0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2011 2013
dbSNP: rs216172
rs216172
0.925 0.040 17 2223210 intron variant G/C snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs2237892
rs2237892
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs2237897
rs2237897
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011