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rs267608499

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608499(-;-)
Make rs267608499(-;G)
Make rs267608499(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031261
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608499
ebirs267608499
HLIrs267608499
Exacrs267608499
Varsomers267608499
Maprs267608499
PheGenIrs267608499
hapmaprs267608499
1000 genomesrs267608499
hgdprs267608499
ensemblrs267608499
gopubmedrs267608499
geneviewrs267608499
scholarrs267608499
googlers267608499
pharmgkbrs267608499
gwascentralrs267608499
openSNPrs267608499
23andMers267608499
23andMe allrs267608499
SNP Nexus

SNPshotrs267608499
SNPdbers267608499
MSV3drs267608499
GWAS Ctlgrs267608499
Max Magnitude0
ClinVar
Risk rs267608499(G;G)
Alt rs267608499(G;G)
Reference rs267608499(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296713dupC
CLNSRC
CLNACC RCV000133162.2,