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rs587783132

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783132(A;T)
Make rs587783132(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154097665
GeneMECP2
is asnp
is mentioned by
dbSNPrs587783132
ebirs587783132
HLIrs587783132
Exacrs587783132
Varsomers587783132
Maprs587783132
PheGenIrs587783132
hapmaprs587783132
1000 genomesrs587783132
hgdprs587783132
ensemblrs587783132
gopubmedrs587783132
geneviewrs587783132
scholarrs587783132
googlers587783132
pharmgkbrs587783132
gwascentralrs587783132
openSNPrs587783132
23andMers587783132
23andMe allrs587783132
SNP Nexus

SNPshotrs587783132
SNPdbers587783132
MSV3drs587783132
GWAS Ctlgrs587783132
Max Magnitude0
ClinVar
Risk rs587783132(G,T;G,T)
Alt rs587783132(G,T;G,T)
Reference rs587783132(A;A)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363122T>A; NC_000023.10:g.153363122T>C
CLNSRC
CLNACC RCV000144804.3, RCV000170280.1, RCV000170279.1,