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rs786205027

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205027(A;T)
Make rs786205027(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154031062
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205027
ebirs786205027
HLIrs786205027
Exacrs786205027
Varsomers786205027
Maprs786205027
PheGenIrs786205027
hapmaprs786205027
1000 genomesrs786205027
hgdprs786205027
ensemblrs786205027
gopubmedrs786205027
geneviewrs786205027
scholarrs786205027
googlers786205027
pharmgkbrs786205027
gwascentralrs786205027
openSNPrs786205027
23andMers786205027
23andMe allrs786205027
SNP Nexus

SNPshotrs786205027
SNPdbers786205027
MSV3drs786205027
GWAS Ctlgrs786205027
Max Magnitude0
ClinVar
Risk rs786205027(T;T)
Alt rs786205027(T;T)
Reference rs786205027(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296513T>A
CLNSRC
CLNACC RCV000170214.1,