rs4775427, LOC107984782

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.
Tonometry
CUI: C0040420
Disease: Tonometry
573 15 61659036 intron variant C/T snv 0.42 0.700 1.000 3 2018 2018