rs3743860, FANCA

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 16 89752083 intron variant T/C snv 0.47 0.700 1.000 3 2018 2018