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rs267608614

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608614(-;-)
Make rs267608614(-;G)
Make rs267608614(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030625
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608614
ebirs267608614
HLIrs267608614
Exacrs267608614
Varsomers267608614
Maprs267608614
PheGenIrs267608614
hapmaprs267608614
1000 genomesrs267608614
hgdprs267608614
ensemblrs267608614
gopubmedrs267608614
geneviewrs267608614
scholarrs267608614
googlers267608614
pharmgkbrs267608614
gwascentralrs267608614
openSNPrs267608614
23andMers267608614
23andMe allrs267608614
SNP Nexus

SNPshotrs267608614
SNPdbers267608614
MSV3drs267608614
GWAS Ctlgrs267608614
Max Magnitude0
ClinVar
Risk rs267608614(G;G)
Alt rs267608614(G;G)
Reference rs267608614(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296077dupC
CLNSRC
CLNACC RCV000132962.2,