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: rs1361270203
rs1361270203
WRN
1.000 0.080 8 31067049 frameshift variant -/CT delins
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		0.700 0