rs776963381, WRN

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.
Werner Syndrome
CUI: C0043119
Disease: Werner Syndrome
71 1.000 0.080 8 31147052 splice acceptor variant G/A;T snv 2.0E-05 0.700 0