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: rs104894864
rs104894864
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057518718
rs1057518718
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1064797104
rs1064797104
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
CCTCAGCTTTTCGCTTCCTGCCGGGG 0.700 CausalMutation CLINVAR
dbSNP: rs1557134378
rs1557134378
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
CCACGG 0.700 CausalMutation CLINVAR
dbSNP: rs1557134481
rs1557134481
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1557134621
rs1557134621
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1557134720
rs1557134720
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557134770
rs1557134770
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.700 CausalMutation CLINVAR
dbSNP: rs1557134779
rs1557134779
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1557134819
rs1557134819
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.700 CausalMutation CLINVAR
dbSNP: rs1557134858
rs1557134858
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557135016
rs1557135016
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.700 CausalMutation CLINVAR
dbSNP: rs1557135039
rs1557135039
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1557135076
rs1557135076
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.700 CausalMutation CLINVAR
dbSNP: rs1557135110
rs1557135110
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
TGCAAAGAGGAGAAGATGCCCAGAGGAGGCTCACT 0.700 CausalMutation CLINVAR
dbSNP: rs1557135125
rs1557135125
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1557135128
rs1557135128
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.700 CausalMutation CLINVAR
dbSNP: rs1557135137
rs1557135137
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557135197
rs1557135197
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
A 0.700 CausalMutation CLINVAR
dbSNP: rs1557135212
rs1557135212
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.700 CausalMutation CLINVAR
dbSNP: rs1557135213
rs1557135213
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
C 0.700 CausalMutation CLINVAR
dbSNP: rs1557135218
rs1557135218
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.700 CausalMutation CLINVAR
dbSNP: rs1557135225
rs1557135225
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
T 0.700 CausalMutation CLINVAR
dbSNP: rs1557135268
rs1557135268
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1557135285
rs1557135285
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0035372
Disease:
Rett Syndrome
G 0.700 CausalMutation CLINVAR