Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs179363900
rs179363900
MECP2
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		C 0.710 CausalMutation CLINVAR

dbSNP: rs179363900
rs179363900
MECP2
CUI: C1846058
Disease: Lubs X-linked mental retardation syndrome
Lubs X-linked mental retardation syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs179363900
rs179363900
MECP2
CUI: C2677682
Disease: Rett Syndrome, Zappella Variant
Rett Syndrome, Zappella Variant 		C 0.700 CausalMutation CLINVAR

dbSNP: rs179363900
rs179363900
MECP2
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		C 0.700 CausalMutation CLINVAR

dbSNP: rs179363900
rs179363900
MECP2
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		C 0.700 CausalMutation CLINVAR

dbSNP: rs179363900
rs179363900
MECP2
CUI: C1968556
Disease: ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS 		C 0.700 CausalMutation CLINVAR