rs6749447, STK39

N. diseases: 2
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 2 168184876 intron variant T/G snv 0.37 0.030 0.667 3 2013 2018
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 2 168184876 intron variant T/G snv 0.37 0.800 1.000 1 2009 2009