Gene: MECP2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569548274
rs1569548274
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs61749721
rs61749721
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1557136758
rs1557136758
MECP2
CT 0.700 CausalMutation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs1557137745
rs1557137745
MECP2
A 0.700 GeneticVariation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs28934906
rs28934906
MECP2
A 0.700 CausalMutation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs61748396
rs61748396
MECP2
C 0.700 CausalMutation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs61749724
rs61749724
MECP2
C 0.700 CausalMutation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs61750240
rs61750240
MECP2
A 0.700 CausalMutation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs61750241
rs61750241
MECP2
G 0.700 CausalMutation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs61751443
rs61751443
MECP2
G 0.700 GeneticVariation CLINVAR Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. 8177735

1993
dbSNP: rs1557136758
rs1557136758
MECP2
CT 0.700 CausalMutation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs1557137745
rs1557137745
MECP2
A 0.700 GeneticVariation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs28934906
rs28934906
MECP2
A 0.700 CausalMutation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs61748396
rs61748396
MECP2
C 0.700 CausalMutation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs61749724
rs61749724
MECP2
C 0.700 CausalMutation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs61750240
rs61750240
MECP2
A 0.700 CausalMutation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs61750241
rs61750241
MECP2
G 0.700 CausalMutation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs61751443
rs61751443
MECP2
G 0.700 GeneticVariation CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514

1999
dbSNP: rs1557136758
rs1557136758
MECP2
CT 0.700 CausalMutation CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019

2001
dbSNP: rs1557137745
rs1557137745
MECP2
A 0.700 GeneticVariation CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019

2001
dbSNP: rs28934906
rs28934906
MECP2
A 0.700 CausalMutation CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019

2001
dbSNP: rs61748396
rs61748396
MECP2
C 0.700 CausalMutation CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019

2001
dbSNP: rs61749724
rs61749724
MECP2
C 0.700 CausalMutation CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019

2001
dbSNP: rs61750240
rs61750240
MECP2
A 0.700 CausalMutation CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019

2001
dbSNP: rs61750241
rs61750241
MECP2
G 0.700 CausalMutation CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019

2001