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rs267608595

From SNPedia

Orientationminus
Geno Mag Summary
(CCCCACC;CCCCACC) 0 common in clinvar
Make rs267608595(-;-)
Make rs267608595(-;CCCCACC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030662
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608595
ebirs267608595
HLIrs267608595
Exacrs267608595
Varsomers267608595
Maprs267608595
PheGenIrs267608595
hapmaprs267608595
1000 genomesrs267608595
hgdprs267608595
ensemblrs267608595
gopubmedrs267608595
geneviewrs267608595
scholarrs267608595
googlers267608595
pharmgkbrs267608595
gwascentralrs267608595
openSNPrs267608595
23andMers267608595
23andMe allrs267608595
SNP Nexus

SNPshotrs267608595
SNPdbers267608595
MSV3drs267608595
GWAS Ctlgrs267608595
Max Magnitude0
ClinVar
Risk rs267608595(;)
Alt rs267608595(;)
Reference rs267608595(CCCCACC;CCCCACC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296113_153296119delGGTGGGG
CLNSRC
CLNACC RCV000132909.2,