Disease: COWDEN SYNDROME 7 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs36023150
rs36023150
Entrez Id: 10483
Gene Symbol: SEC23B
SEC23B
CUI: C4225179
Disease:
COWDEN SYNDROME 7 		0.700 GeneticVariation UNIPROT Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer. 26522472 2015