rs10491334, CAMK4

N. diseases: 1
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 5 111436706 intron variant C/T snv 0.14 0.010 1.000 1 2016 2016