MECP2, methyl-CpG binding protein 2, 4204

N. diseases: 664; N. variants: 387
Disease: Angelman Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557135251
rs1557135251
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs267608426
rs267608426
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		C 0.700 CausalMutation CLINVAR
dbSNP: rs267608434
rs267608434
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		C 0.700 CausalMutation CLINVAR
dbSNP: rs28934904
rs28934904
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs28934906
rs28934906
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs28935468
rs28935468
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs61748396
rs61748396
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		C 0.700 CausalMutation CLINVAR
dbSNP: rs61750241
rs61750241
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		G 0.700 CausalMutation CLINVAR
dbSNP: rs63749748
rs63749748
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0162635
Disease:
Angelman Syndrome 		T 0.700 CausalMutation CLINVAR