rs794728947, SDHB

N. diseases: 4
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.925 0.080 1 17033135 frameshift variant -/G delins 4.0E-06 0.700 1.000 1 2002 2002
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.925 0.080 1 17033135 frameshift variant -/G delins 4.0E-06 0.700 0
PARAGANGLIOMAS 4
CUI: C1861848
Disease: PARAGANGLIOMAS 4
67 0.925 0.080 1 17033135 frameshift variant -/G delins 4.0E-06 0.700 0
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.925 0.080 1 17033135 frameshift variant -/G delins 4.0E-06 0.700 0