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: rs1902341
rs1902341
3 31754078 intron variant C/T snv 0.49
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.810 1.000 1 2010 2010
dbSNP: rs653178
rs653178
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.800 1.000 1 2014 2014
dbSNP: rs2074633
rs2074633
7 18996297 3 prime UTR variant T/A;C snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2015 2015
dbSNP: rs6842241
rs6842241
0.925 0.080 4 147479667 upstream gene variant C/A snv 0.22
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2015 2015
dbSNP: rs9584669
rs9584669
13 97711228 intergenic variant T/C snv 0.19
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.710 1.000 1 2015 2015
dbSNP: rs10046574
rs10046574
7 135485722 intron variant C/T snv 7.4E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs10428206
rs10428206
3 74485377 intron variant T/C snv 1.5E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs10467515
rs10467515
13 52927172 regulatory region variant A/G snv 1.2E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs10484876
rs10484876
6 52389351 intron variant C/T snv 0.14
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs10979314
rs10979314
9 108310149 intergenic variant G/A snv 7.2E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11039100
rs11039100
11 5805773 intron variant T/C snv 0.11
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11077983
rs11077983
17 82227312 upstream gene variant C/G;T snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11190074
rs11190074
10 99361961 intron variant A/G snv 8.7E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11206019
rs11206019
1 52794278 intron variant G/T snv 0.16
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11220138
rs11220138
11 125585927 intron variant C/T snv 7.7E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11466653
rs11466653
1.000 0.080 4 38774614 missense variant A/G snv 6.4E-02 4.1E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11512640
rs11512640
11 125556427 intron variant G/T snv 7.7E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11819158
rs11819158
10 99418299 intron variant G/T snv 2.3E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs11942139
rs11942139
4 6429357 intron variant T/C snv 2.5E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs12257301
rs12257301
10 86655778 intron variant G/A snv 7.1E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs12335314
rs12335314
8 124550784 intron variant T/G snv 1.7E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs12445943
rs12445943
16 78775175 intron variant G/A snv 0.17
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs13389599
rs13389599
2 76861472 intron variant T/C snv 2.6E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs1539189
rs1539189
20 1966633 intron variant A/G snv 2.0E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs1638665
rs1638665
10 117414434 regulatory region variant T/C snv 2.9E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.700 1.000 1 2016 2016