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rs267608638

From SNPedia

Orientationminus
Geno Mag Summary
(AGAG;AGAG) 0 common in clinvar
Make rs267608638(-;-)
Make rs267608638(-;AGAG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030375
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608638
ebirs267608638
HLIrs267608638
Exacrs267608638
Varsomers267608638
Maprs267608638
PheGenIrs267608638
hapmaprs267608638
1000 genomesrs267608638
hgdprs267608638
ensemblrs267608638
gopubmedrs267608638
geneviewrs267608638
scholarrs267608638
googlers267608638
pharmgkbrs267608638
gwascentralrs267608638
openSNPrs267608638
23andMers267608638
23andMe allrs267608638
SNP Nexus

SNPshotrs267608638
SNPdbers267608638
MSV3drs267608638
GWAS Ctlgrs267608638
Max Magnitude0
ClinVar
Risk rs267608638(;)
Alt rs267608638(;)
Reference rs267608638(AGAG;AGAG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153295826_153295829delCTCT
CLNSRC
CLNACC RCV000133013.2,