rs3773643, TGFBR2

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.
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 3 30668751 intron variant A/G snv 0.19 0.700 1.000 1 2007 2007
Tonometry
CUI: C0040420
Disease: Tonometry
573 3 30668751 intron variant A/G snv 0.19 0.700 1.000 1 2007 2007