MECP2, methyl-CpG binding protein 2, 4204

N. diseases: 664; N. variants: 387
Disease: Mental Retardation, X-Linked, Syndromic 13 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267608590
rs267608590
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C1968550
Disease:
Mental Retardation, X-Linked, Syndromic 13 		A 0.700 CausalMutation CLINVAR