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: rs779530981
rs779530981
PTEN
1.000 0.160 10 87933035 missense variant C/A snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2010 2010
dbSNP: rs779530981
rs779530981
PTEN
1.000 0.160 10 87933035 missense variant C/A snv
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		0.010 1.000 1 2007 2007
dbSNP: rs779530981
rs779530981
PTEN
1.000 0.160 10 87933035 missense variant C/A snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2010 2010
dbSNP: rs779530981
rs779530981
PTEN
1.000 0.160 10 87933035 missense variant C/A snv
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms 		0.010 1.000 1 2007 2007