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rs267608424

From SNPedia

Orientationminus
Geno Mag Summary
(AAGAAGA;AAGAAGA) 0 common in clinvar
Make rs267608424(-;-)
Make rs267608424(-;AAGAAGA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032471
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608424
ebirs267608424
HLIrs267608424
Exacrs267608424
Varsomers267608424
Maprs267608424
PheGenIrs267608424
hapmaprs267608424
1000 genomesrs267608424
hgdprs267608424
ensemblrs267608424
gopubmedrs267608424
geneviewrs267608424
scholarrs267608424
googlers267608424
pharmgkbrs267608424
gwascentralrs267608424
openSNPrs267608424
23andMers267608424
23andMe allrs267608424
SNP Nexus

SNPshotrs267608424
SNPdbers267608424
MSV3drs267608424
GWAS Ctlgrs267608424
Max Magnitude0
ClinVar
Risk rs267608424(;)
Alt rs267608424(;)
Reference rs267608424(AAGAAGA;AAGAAGA)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297922_153297928delTCTTCTT
CLNSRC
CLNACC RCV000132849.2,