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rs267608416

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608416(-;-)
Make rs267608416(-;A)
Make rs267608416(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032533
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608416
ebirs267608416
HLIrs267608416
Exacrs267608416
Varsomers267608416
Maprs267608416
PheGenIrs267608416
hapmaprs267608416
1000 genomesrs267608416
hgdprs267608416
ensemblrs267608416
gopubmedrs267608416
geneviewrs267608416
scholarrs267608416
googlers267608416
pharmgkbrs267608416
gwascentralrs267608416
openSNPrs267608416
23andMers267608416
23andMe allrs267608416
SNP Nexus

SNPshotrs267608416
SNPdbers267608416
MSV3drs267608416
GWAS Ctlgrs267608416
Max Magnitude0
ClinVar
Risk rs267608416(A;A)
Alt rs267608416(A;A)
Reference rs267608416(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297985dupT
CLNSRC
CLNACC RCV000133145.2,