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rs267608476

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608476(-;-)
Make rs267608476(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031408
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608476
ebirs267608476
HLIrs267608476
Exacrs267608476
Varsomers267608476
Maprs267608476
PheGenIrs267608476
hapmaprs267608476
1000 genomesrs267608476
hgdprs267608476
ensemblrs267608476
gopubmedrs267608476
geneviewrs267608476
scholarrs267608476
googlers267608476
pharmgkbrs267608476
gwascentralrs267608476
openSNPrs267608476
23andMers267608476
23andMe allrs267608476
SNP Nexus

SNPshotrs267608476
SNPdbers267608476
MSV3drs267608476
GWAS Ctlgrs267608476
Max Magnitude0
ClinVar
Risk rs267608476(;)
Alt rs267608476(;)
Reference rs267608476(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296859delC
CLNSRC
CLNACC RCV000133103.2,