Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113993961
rs113993961
WRN
1.000 0.080 8 31141680 splice acceptor variant G/C snv 4.0E-06
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		0.700 1.000 5 1996 2006