rs7687961, CYP4V2

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.
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 4 186200855 intron variant C/A snv 0.72 0.700 1.000 1 2013 2013