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rs267608612

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608612(-;-)
Make rs267608612(-;C)
Make rs267608612(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030630
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608612
ebirs267608612
HLIrs267608612
Exacrs267608612
Varsomers267608612
Maprs267608612
PheGenIrs267608612
hapmaprs267608612
1000 genomesrs267608612
hgdprs267608612
ensemblrs267608612
gopubmedrs267608612
geneviewrs267608612
scholarrs267608612
googlers267608612
pharmgkbrs267608612
gwascentralrs267608612
openSNPrs267608612
23andMers267608612
23andMe allrs267608612
SNP Nexus

SNPshotrs267608612
SNPdbers267608612
MSV3drs267608612
GWAS Ctlgrs267608612
Max Magnitude0
ClinVar
Risk rs267608612(C;C)
Alt rs267608612(C;C)
Reference rs267608612(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296082dupG
CLNSRC
CLNACC RCV000132958.2,