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: 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
dbSNP: rs173539
rs173539
0.882 0.080 16 56954132 intergenic variant C/T snv 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs1800775
rs1800775
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1800961
rs1800961
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: rs2083637
rs2083637
0.925 0.080 8 20007664 intergenic variant A/G snv 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs2156552
rs2156552
1.000 0.040 18 49655298 downstream gene variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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
dbSNP: rs2250781
rs2250781
1.000 0.040 10 89247713 5 prime UTR variant C/A snv 0.59
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs2254287
rs2254287
1.000 0.040 6 33176171 intron variant C/A;G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011