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rs267608444

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs267608444(-;-)
Make rs267608444(-;CA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032325
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608444
ebirs267608444
HLIrs267608444
Exacrs267608444
Varsomers267608444
Maprs267608444
PheGenIrs267608444
hapmaprs267608444
1000 genomesrs267608444
hgdprs267608444
ensemblrs267608444
gopubmedrs267608444
geneviewrs267608444
scholarrs267608444
googlers267608444
pharmgkbrs267608444
gwascentralrs267608444
openSNPrs267608444
23andMers267608444
23andMe allrs267608444
SNP Nexus

SNPshotrs267608444
SNPdbers267608444
MSV3drs267608444
GWAS Ctlgrs267608444
Max Magnitude0
ClinVar
Risk rs267608444(;)
Alt rs267608444(;)
Reference rs267608444(CA;CA)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297776_153297777delTG
CLNSRC
CLNACC RCV000133042.2,