Source: GWASDB

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: rs7914558
rs7914558
0.851 0.040 10 103016151 intron variant G/A snv 0.40
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.830 1.000 1 2011 2020
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.800 1.000 1 2010 2010
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
dbSNP: rs1890185
rs1890185
10 102988961 intron variant A/G snv 0.41
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.800 1.000 1 2013 2013
dbSNP: rs7914558
rs7914558
0.851 0.040 10 103016151 intron variant G/A snv 0.40
Attention deficit hyperactivity disorder
0.800 1.000 1 2013 2013
dbSNP: rs11191548
rs11191548
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 3 2011 2011
dbSNP: rs11191548
rs11191548
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
0.700 1.000 2 2009 2011
dbSNP: rs11191548
rs11191548
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs12411886
rs12411886
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2009 2009
dbSNP: rs12411886
rs12411886
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.700 1.000 1 2010 2010
dbSNP: rs12411886
rs12411886
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
0.700 1.000 1 2013 2013
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2009 2009
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2014 2014
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
0.700 1.000 1 2013 2013