Gene: MECP2 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61750241
rs61750241
MECP2
G 0.700 CausalMutation CLINVAR Apneic crises: a clue for MECP2 testing in severe neonatal hypotonia-respiratory failure. 22497713

2012
dbSNP: rs61750241
rs61750241
MECP2
G 0.700 CausalMutation CLINVAR Functional consequences of Rett syndrome mutations on human MeCP2. 11058114

2000
dbSNP: rs61750241
rs61750241
MECP2
G 0.700 CausalMutation CLINVAR Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots. 10577905

1999
dbSNP: rs1557135315
rs1557135315
MECP2
C 0.700 CausalMutation CLINVAR

dbSNP: rs179363900
rs179363900
MECP2
C 0.700 CausalMutation CLINVAR

dbSNP: rs28934906
rs28934906
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs61749721
rs61749721
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs61750240
rs61750240
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs61751362
rs61751362
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs61752992
rs61752992
MECP2
G 0.700 CausalMutation CLINVAR