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rs267608610

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608610(-;-)
Make rs267608610(-;A)
Make rs267608610(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030637
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608610
ebirs267608610
HLIrs267608610
Exacrs267608610
Varsomers267608610
Maprs267608610
PheGenIrs267608610
hapmaprs267608610
1000 genomesrs267608610
hgdprs267608610
ensemblrs267608610
gopubmedrs267608610
geneviewrs267608610
scholarrs267608610
googlers267608610
pharmgkbrs267608610
gwascentralrs267608610
openSNPrs267608610
23andMers267608610
23andMe allrs267608610
SNP Nexus

SNPshotrs267608610
SNPdbers267608610
MSV3drs267608610
GWAS Ctlgrs267608610
Max Magnitude0
ClinVar
Risk rs267608610(A;A)
Alt rs267608610(A;A)
Reference rs267608610(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296089dupT
CLNSRC
CLNACC RCV000132954.2,