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rs267608442

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608442(-;-)
Make rs267608442(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032351
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608442
ebirs267608442
HLIrs267608442
Exacrs267608442
Varsomers267608442
Maprs267608442
PheGenIrs267608442
hapmaprs267608442
1000 genomesrs267608442
hgdprs267608442
ensemblrs267608442
gopubmedrs267608442
geneviewrs267608442
scholarrs267608442
googlers267608442
pharmgkbrs267608442
gwascentralrs267608442
openSNPrs267608442
23andMers267608442
23andMe allrs267608442
SNP Nexus

SNPshotrs267608442
SNPdbers267608442
MSV3drs267608442
GWAS Ctlgrs267608442
Max Magnitude0
ClinVar
Risk rs267608442(;)
Alt rs267608442(;)
Reference rs267608442(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297802delG
CLNSRC
CLNACC RCV000133038.2,