Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28934908
rs28934908
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0036857
Disease:
Severe intellectual disability
0.010 GeneticVariation BEFREE In a family study, the A140V mutation was found to segregate in the affected daughter and in four adult sons with severe mental retardation. 11007980 2000