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rs267608417

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608417(-;-)
Make rs267608417(-;A)
Make rs267608417(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032527
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608417
ebirs267608417
HLIrs267608417
Exacrs267608417
Varsomers267608417
Maprs267608417
PheGenIrs267608417
hapmaprs267608417
1000 genomesrs267608417
hgdprs267608417
ensemblrs267608417
gopubmedrs267608417
geneviewrs267608417
scholarrs267608417
googlers267608417
pharmgkbrs267608417
gwascentralrs267608417
openSNPrs267608417
23andMers267608417
23andMe allrs267608417
SNP Nexus

SNPshotrs267608417
SNPdbers267608417
MSV3drs267608417
GWAS Ctlgrs267608417
Max Magnitude0
ClinVar
Risk rs267608417(A;A)
Alt rs267608417(A;A)
Reference rs267608417(;)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297979dupT
CLNSRC
CLNACC RCV000133164.2, RCV000194653.1,