rs121909235, PTEN

N. diseases: 8
Source: ALL
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.
GLIOMA SUSCEPTIBILITY 2
CUI: C2751642
Disease: GLIOMA SUSCEPTIBILITY 2
6 0.851 0.240 10 87957919 missense variant G/A snv 0.700 1.000 1 2002 2002
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2018 2018
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
CUI: C1832661
Disease: ANOPHTHALMIA AND PULMONARY HYPOPLASIA
80 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2018 2018
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2002 2002
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2018 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2002 2002
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2018 2018
PTEN Hamartoma Tumor Syndrome
CUI: C1959582
Disease: PTEN Hamartoma Tumor Syndrome
194 0.851 0.240 10 87957919 missense variant G/A snv 0.010 1.000 1 2018 2018