rs587782350, PTEN

N. diseases: 8
Source: CURATED ×
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.
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
107 0.776 0.160 10 87957955 missense variant C/T snv 0.810 1.000 30 1997 2017
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.776 0.160 10 87957955 missense variant C/T snv 0.700 1.000 12 1999 2017
PTEN Hamartoma Tumor Syndrome
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
193 0.776 0.160 10 87957955 missense variant C/T snv 0.700 1.000 10 1999 2017
Cerebellar Granule Cell Hypertrophy and Megalencephaly
CUI: C1834712
Disease: Cerebellar Granule Cell Hypertrophy and Megalencephaly
56 0.776 0.160 10 87957955 missense variant C/T snv 0.700 1.000 8 1999 2017
CEREBELLOPARENCHYMAL DISORDER VI
CUI: C1834711
Disease: CEREBELLOPARENCHYMAL DISORDER VI
56 0.776 0.160 10 87957955 missense variant C/T snv 0.700 1.000 8 1999 2017
Lhermitte-Duclos disease
CUI: C0391826
Disease: Lhermitte-Duclos disease
58 0.776 0.160 10 87957955 missense variant C/T snv 0.700 1.000 8 1999 2017
Proteus-Like Syndrome (disorder)
CUI: C1866398
Disease: Proteus-Like Syndrome (disorder)
56 0.776 0.160 10 87957955 missense variant C/T snv 0.700 1.000 8 1999 2017
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
CUI: C1866376
Disease: Pten Hamartoma Tumor Syndrome With Granular Cell Tumor
56 0.776 0.160 10 87957955 missense variant C/T snv 0.700 1.000 8 1999 2017