rs772551056, SDHB

N. diseases: 9
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.
PARAGANGLIOMAS 4
CUI: C1861848
Disease: PARAGANGLIOMAS 4
67 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.800 1.000 24 2003 2017
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.800 1.000 11 2003 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.700 1.000 14 2002 2018
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.700 1.000 11 2003 2016
Hereditary Paraganglioma-Pheochromocytoma Syndrome
98 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.700 1.000 9 2002 2016
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
34 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.700 0
Malignant Paraganglionic Neoplasm
CUI: C1533592
Disease: Malignant Paraganglionic Neoplasm
3 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2008 2008
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2008 2008
Paraganglioma
CUI: C0030421
Disease: Paraganglioma
36 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2008 2008