Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61749715
rs61749715
MECP2
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		A 0.800 CausalMutation CLINVAR

dbSNP: rs61749715
rs61749715
MECP2
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		C 0.800 CausalMutation CLINVAR