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: rs12670798
rs12670798
1.000 0.040 7 21567734 intron variant T/C snv 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs12678919
rs12678919
0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs12779790
rs12779790
0.882 0.120 10 12286011 intergenic variant A/G snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs12946454
rs12946454
0.925 0.040 17 45130754 intron variant A/T snv 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs13015955
rs13015955
1.000 0.040 2 22599287 intergenic variant G/A snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs13161895
rs13161895
1.000 0.040 5 180044201 intron variant C/T snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs13266634
rs13266634
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs1378942
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs1501908
rs1501908
1.000 0.040 5 156971158 intergenic variant G/A;C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1530440
rs1530440
1.000 0.040 10 61764833 intron variant C/T snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1532085
rs1532085
0.882 0.080 15 58391167 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1532624
rs1532624
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs1614866
rs1614866
1.000 0.040 1 211527316 regulatory region variant G/A snv 7.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs16965039
rs16965039
1.000 0.040 16 57013387 non coding transcript exon variant T/C snv 5.6E-02
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: rs16996148
rs16996148
0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs16998073
rs16998073
0.925 0.120 4 80263187 upstream gene variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs17036101
rs17036101
0.925 0.120 3 12236345 regulatory region variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011