Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17222919
rs17222919
1.000 0.080 13 30734192 intron variant T/A;G snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.040 0.750 4 2011 2019
dbSNP: rs10507391
rs10507391
0.776 0.320 13 30737959 intron variant A/T snv 0.52
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.030 0.667 3 2015 2019
dbSNP: rs4073259
rs4073259
0.882 0.160 13 30732134 intron variant G/A snv 0.49
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.030 0.333 3 2012 2019
dbSNP: rs9579646
rs9579646
0.851 0.160 13 30736442 intron variant G/A;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.030 1.000 3 2007 2016
dbSNP: rs17222814
rs17222814
1.000 0.080 13 30725416 intron variant G/A snv 6.9E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.020 0.500 2 2008 2019
dbSNP: rs4769874
rs4769874
0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.020 0.500 2 2007 2019
dbSNP: rs9551963
rs9551963
0.851 0.160 13 30758410 intron variant A/C;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.020 0.500 2 2012 2019
dbSNP: rs12429692
rs12429692
1.000 0.080 13 30738041 intron variant A/T snv 0.24
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4293222
rs4293222
1.000 0.080 13 30737636 intron variant C/A;G snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs9315050
rs9315050
1.000 0.080 13 30761908 intron variant A/G snv 0.11
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012