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rs786205045

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205045(C;T)
Make rs786205045(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154097618
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205045
ebirs786205045
HLIrs786205045
Exacrs786205045
Varsomers786205045
Maprs786205045
PheGenIrs786205045
hapmaprs786205045
1000 genomesrs786205045
hgdprs786205045
ensemblrs786205045
gopubmedrs786205045
geneviewrs786205045
scholarrs786205045
googlers786205045
pharmgkbrs786205045
gwascentralrs786205045
openSNPrs786205045
23andMers786205045
23andMe allrs786205045
SNP Nexus

SNPshotrs786205045
SNPdbers786205045
MSV3drs786205045
GWAS Ctlgrs786205045
Max Magnitude0
ClinVar
Risk rs786205045(T;T)
Alt rs786205045(T;T)
Reference rs786205045(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363075G>A
CLNSRC
CLNACC RCV000170291.1,