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rs267608601

From SNPedia

Orientationminus
Geno Mag Summary
(CACCTCCACCTGAGCCC;CACCTCCACCTGAGCCC) 0 common in clinvar
Make rs267608601(-;-)
Make rs267608601(-;CACCTCCACCTGAGCCC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030649
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608601
ebirs267608601
HLIrs267608601
Exacrs267608601
Varsomers267608601
Maprs267608601
PheGenIrs267608601
hapmaprs267608601
1000 genomesrs267608601
hgdprs267608601
ensemblrs267608601
gopubmedrs267608601
geneviewrs267608601
scholarrs267608601
googlers267608601
pharmgkbrs267608601
gwascentralrs267608601
openSNPrs267608601
23andMers267608601
23andMe allrs267608601
SNP Nexus

SNPshotrs267608601
SNPdbers267608601
MSV3drs267608601
GWAS Ctlgrs267608601
Max Magnitude0
ClinVar
Risk rs267608601(;)
Alt rs267608601(;)
Reference rs267608601(CACCTCCACCTGAGCCC;CACCTCCACCTGAGCCC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296100_153296116del17
CLNSRC
CLNACC RCV000132926.2,