Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61748404
rs61748404
MECP2
0.810 GeneticVariation BEFREE This case broadens the genotype-phenotype correlation between the P152R mutation 2MECP2-associated Rett syndrome. 23859859

2013