MECP2, methyl-CpG binding protein 2, 4204

N. diseases: 664; N. variants: 387
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28934905
rs28934905
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.810 CausalMutation CLINVAR
dbSNP: rs61748390
rs61748390
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.810 CausalMutation CLINVAR
dbSNP: rs28935168
rs28935168
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs61749715
rs61749715
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs61749715
rs61749715
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs61749723
rs61749723
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs61751443
rs61751443
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs61751449
rs61751449
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs61754421
rs61754421
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs61754452
rs61754452
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs61754453
rs61754453
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs61754453
rs61754453
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs61754453
rs61754453
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs61754457
rs61754457
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs61751364
rs61751364
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.770 CausalMutation CLINVAR
dbSNP: rs61748421
rs61748421
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.740 CausalMutation CLINVAR
dbSNP: rs61751362
rs61751362
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.730 GeneticVariation CLINVAR
dbSNP: rs61749721
rs61749721
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.720 GeneticVariation CLINVAR
dbSNP: rs61751444
rs61751444
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.720 GeneticVariation CLINVAR
dbSNP: rs179363900
rs179363900
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.710 CausalMutation CLINVAR
dbSNP: rs267608475
rs267608475
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.710 CausalMutation CLINVAR
dbSNP: rs267608591
rs267608591
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.710 CausalMutation CLINVAR
dbSNP: rs28934908
rs28934908
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.710 GeneticVariation CLINVAR
dbSNP: rs61751367
rs61751367
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.710 CausalMutation CLINVAR
dbSNP: rs786205045
rs786205045
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.710 CausalMutation CLINVAR