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rs267608518

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608518(-;-)
Make rs267608518(-;C)
Make rs267608518(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031107
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608518
ebirs267608518
HLIrs267608518
Exacrs267608518
Varsomers267608518
Maprs267608518
PheGenIrs267608518
hapmaprs267608518
1000 genomesrs267608518
hgdprs267608518
ensemblrs267608518
gopubmedrs267608518
geneviewrs267608518
scholarrs267608518
googlers267608518
pharmgkbrs267608518
gwascentralrs267608518
openSNPrs267608518
23andMers267608518
23andMe allrs267608518
SNP Nexus

SNPshotrs267608518
SNPdbers267608518
MSV3drs267608518
GWAS Ctlgrs267608518
Max Magnitude0
ClinVar
Risk rs267608518(C;C)
Alt rs267608518(C;C)
Reference rs267608518(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296559dupG
CLNSRC
CLNACC RCV000133212.2,