rs7635832, FNDC3B

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 3 172271486 intron variant T/G snv 0.22 0.700 1.000 3 2017 2018