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: rs10042590
rs10042590
5 88477501 intron variant G/A snv 5.8E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10059884
rs10059884
5 32832368 regulatory region variant C/A;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs1009358
rs1009358
1.000 0.080 2 65049318 intron variant T/C snv 0.40
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10107066
rs10107066
8 26542619 intron variant G/C snv 0.29
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10224210
rs10224210
1.000 0.040 7 151716108 intron variant T/C snv 0.21
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs1030431
rs1030431
8 58399138 intergenic variant A/G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10409243
rs10409243
19 10222312 3 prime UTR variant C/A;G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs1044486
rs1044486
17 78796097 3 prime UTR variant G/A snv 0.41
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs1047964
rs1047964
11 117286177 3 prime UTR variant G/A;C;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.710 1.000 1 2011 2011
dbSNP: rs1048070
rs1048070
9 14735055 3 prime UTR variant T/C snv 0.46
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10500326
rs10500326
16 4868325 intron variant G/T snv 0.21
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10740995
rs10740995
10 18156159 intron variant G/A;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs1074703
rs1074703
8 101803258 intron variant C/A snv 0.63
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10748798
rs10748798
10 100794914 intron variant C/T snv 0.91
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10769254
rs10769254
11 47340914 intron variant G/C snv 0.27
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10786156
rs10786156
10 94254865 intron variant C/G snv 0.44 0.47
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10816914
rs10816914
9 109998608 intron variant G/A snv 0.40
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10821967
rs10821967
10 62182180 downstream gene variant A/G snv 0.51
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10824134
rs10824134
ADK
10 74261866 intron variant T/C snv 0.48
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10832571
rs10832571
11 16239678 intron variant C/T snv 0.16
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10849891
rs10849891
12 121473799 intron variant T/A;G snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10850407
rs10850407
12 114940232 intergenic variant T/G snv 0.24
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10872673
rs10872673
6 151534458 intron variant G/T snv 0.45
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10882397
rs10882397
10 94132902 intron variant C/A snv 0.52
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs10911021
rs10911021
0.807 0.160 1 182112825 intron variant C/T snv 0.36
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.710 1.000 1 2013 2016