rs786203251, SDHB

N. diseases: 5
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.
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.882 0.080 1 17022649 missense variant G/A;T snv 0.700 1.000 10 1992 2013
PARAGANGLIOMAS 4
CUI: C1861848
Disease: PARAGANGLIOMAS 4
67 0.882 0.080 1 17022649 missense variant G/A;T snv 0.700 1.000 10 1992 2013
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.882 0.080 1 17022649 missense variant G/A;T snv 0.700 1.000 10 1992 2013
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.882 0.080 1 17022649 missense variant G/A;T snv 0.700 1.000 9 2004 2015
Carotid Body Paraganglioma
CUI: C0007279
Disease: Carotid Body Paraganglioma
4 0.882 0.080 1 17022649 missense variant G/A;T snv 0.010 1.000 1 2006 2006