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rs267608506

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608506(-;-)
Make rs267608506(-;A)
Make rs267608506(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031219
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608506
ebirs267608506
HLIrs267608506
Exacrs267608506
Varsomers267608506
Maprs267608506
PheGenIrs267608506
hapmaprs267608506
1000 genomesrs267608506
hgdprs267608506
ensemblrs267608506
gopubmedrs267608506
geneviewrs267608506
scholarrs267608506
googlers267608506
pharmgkbrs267608506
gwascentralrs267608506
openSNPrs267608506
23andMers267608506
23andMe allrs267608506
SNP Nexus

SNPshotrs267608506
SNPdbers267608506
MSV3drs267608506
GWAS Ctlgrs267608506
Max Magnitude0
ClinVar
Risk rs267608506(A;A)
Alt rs267608506(A;A)
Reference rs267608506(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296670_153296671insT
CLNSRC
CLNACC RCV000133173.2,