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rs267608438

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608438(C;G)
Make rs267608438(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032381
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608438
ebirs267608438
HLIrs267608438
Exacrs267608438
Varsomers267608438
Maprs267608438
PheGenIrs267608438
hapmaprs267608438
1000 genomesrs267608438
hgdprs267608438
ensemblrs267608438
gopubmedrs267608438
geneviewrs267608438
scholarrs267608438
googlers267608438
pharmgkbrs267608438
gwascentralrs267608438
openSNPrs267608438
23andMers267608438
23andMe allrs267608438
SNP Nexus

SNPshotrs267608438
SNPdbers267608438
MSV3drs267608438
GWAS Ctlgrs267608438
Max Magnitude0
ClinVar
Risk rs267608438(G;G)
Alt rs267608438(G;G)
Reference rs267608438(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297832G>C
CLNSRC
CLNACC RCV000133031.2,