rs139455627, TSPEAR

N. diseases: 14
Disease: Sagittal craniosynostosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sagittal craniosynostosis
CUI: C0432123
Disease: Sagittal craniosynostosis
0.700 GeneticVariation CLINVAR Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. 27736875 2016