rs12258967, CACNB2

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 10 18439030 intron variant C/G;T snv 0.700 1.000 2 2019 2019
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 10 18439030 intron variant C/G;T snv 0.700 1.000 1 2011 2011
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 10 18439030 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 10 18439030 intron variant C/G;T snv 0.700 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 10 18439030 intron variant C/G;T snv 0.010 1.000 1 2018 2018