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rs267608571

From SNPedia

Orientationminus
Geno Mag Summary
(CCCGTGCC;CCCGTGCC) 0 common in clinvar
Make rs267608571(-;-)
Make rs267608571(-;CCCGTGCC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030686
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608571
ebirs267608571
HLIrs267608571
Exacrs267608571
Varsomers267608571
Maprs267608571
PheGenIrs267608571
hapmaprs267608571
1000 genomesrs267608571
hgdprs267608571
ensemblrs267608571
gopubmedrs267608571
geneviewrs267608571
scholarrs267608571
googlers267608571
pharmgkbrs267608571
gwascentralrs267608571
openSNPrs267608571
23andMers267608571
23andMe allrs267608571
SNP Nexus

SNPshotrs267608571
SNPdbers267608571
MSV3drs267608571
GWAS Ctlgrs267608571
Max Magnitude0
ClinVar
Risk rs267608571(;)
Alt rs267608571(;)
Reference rs267608571(CCCGTGCC;CCCGTGCC)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MECP2
CLNDBN Mental retardation, X-linked, syndromic 13
Reversed 1
HGVS NC_000023.10:g.153296137_153296144delGGCACGGG
CLNSRC
CLNACC RCV000132867.2,