Disease: SECKEL SYNDROME 10 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757613817
rs757613817
Entrez Id: 286053
Gene Symbol: NSMCE2
NSMCE2
CUI: C4310647
Disease:
SECKEL SYNDROME 10 		A 0.700 CausalMutation CLINVAR