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rs267608597

From SNPedia

Orientationminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs267608597(CC;TA)
Make rs267608597(TA;TA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030665
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608597
ebirs267608597
HLIrs267608597
Exacrs267608597
Varsomers267608597
Maprs267608597
PheGenIrs267608597
hapmaprs267608597
1000 genomesrs267608597
hgdprs267608597
ensemblrs267608597
gopubmedrs267608597
geneviewrs267608597
scholarrs267608597
googlers267608597
pharmgkbrs267608597
gwascentralrs267608597
openSNPrs267608597
23andMers267608597
23andMe allrs267608597
SNP Nexus

SNPshotrs267608597
SNPdbers267608597
MSV3drs267608597
GWAS Ctlgrs267608597
Max Magnitude0
ClinVar
Risk rs267608597(TA;TA)
Alt rs267608597(TA;TA)
Reference rs267608597(CC;CC)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MECP2
CLNDBN Mental retardation, X-linked, syndromic 13
Reversed 1
HGVS NC_000023.10:g.153296116_153296117delGGinsTA
CLNSRC
CLNACC RCV000132921.2,