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: rs11014166
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.800 1.000 1 2009 2009
dbSNP: rs17691888
rs17691888
CACNB2
1.000 0.040 10 18445599 intron variant G/A snv 0.16
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2013 2019
dbSNP: rs2799573
rs2799573
CACNB2
0.851 0.040 10 18312999 intron variant T/C snv 0.20
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs11014166
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.710 1.000 1 2010 2011
dbSNP: rs11014166
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs11014166
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2009 2009
dbSNP: rs11014166
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2009 2009
dbSNP: rs12258967
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1813353
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1813353
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs7069923
rs7069923
CACNB2
10 18441439 intron variant C/T snv 0.36
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009
dbSNP: rs8181477
rs8181477
CACNB2
10 18493951 intron variant A/C snv 0.43
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012