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rs267608411

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608411(C;G)
Make rs267608411(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032563
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608411
ebirs267608411
HLIrs267608411
Exacrs267608411
Varsomers267608411
Maprs267608411
PheGenIrs267608411
hapmaprs267608411
1000 genomesrs267608411
hgdprs267608411
ensemblrs267608411
gopubmedrs267608411
geneviewrs267608411
scholarrs267608411
googlers267608411
pharmgkbrs267608411
gwascentralrs267608411
openSNPrs267608411
23andMers267608411
23andMe allrs267608411
SNP Nexus

SNPshotrs267608411
SNPdbers267608411
MSV3drs267608411
GWAS Ctlgrs267608411
Max Magnitude0
ClinVar
Risk rs267608411(G;G)
Alt rs267608411(G;G)
Reference rs267608411(C;C)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153298014G>C
CLNSRC
CLNACC RCV000144095.1, RCV000170187.2,