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: rs786202055
rs786202055
TP53
17 7673714 frameshift variant C/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 0
dbSNP: rs786202055
rs786202055
TP53
17 7673714 frameshift variant C/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2015 2015