rs786201095, SDHB

N. diseases: 7
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.
Hereditary Paraganglioma-Pheochromocytoma Syndrome
CUI: C1708353
Disease: Hereditary Paraganglioma-Pheochromocytoma Syndrome
98 0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 0.700 1.000 18 2005 2018
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 0.700 1.000 17 2005 2018
PARAGANGLIOMAS 4
CUI: C1861848
Disease: PARAGANGLIOMAS 4
67 0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 0.700 1.000 12 2005 2015
Pheochromocytoma
CUI: C0031511
Disease: Pheochromocytoma
186 0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 0.700 1.000 12 2005 2015
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 0.700 1.000 7 2005 2017
Carney Triad
CUI: C1858592
Disease: Carney Triad
6 0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 0.700 0
Pulmonary chondroma
CUI: C3203483
Disease: Pulmonary chondroma
6 0.827 0.160 1 17028643 missense variant A/C snv 1.2E-05 0.700 0