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rs267608492

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608492(C;G)
Make rs267608492(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154031310
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608492
ebirs267608492
HLIrs267608492
Exacrs267608492
Varsomers267608492
Maprs267608492
PheGenIrs267608492
hapmaprs267608492
1000 genomesrs267608492
hgdprs267608492
ensemblrs267608492
gopubmedrs267608492
geneviewrs267608492
scholarrs267608492
googlers267608492
pharmgkbrs267608492
gwascentralrs267608492
openSNPrs267608492
23andMers267608492
23andMe allrs267608492
SNP Nexus

SNPshotrs267608492
SNPdbers267608492
MSV3drs267608492
GWAS Ctlgrs267608492
Max Magnitude0
ClinVar
Risk rs267608492(G;G)
Alt rs267608492(G;G)
Reference rs267608492(C;C)
Significance Pathogenic
Disease not specified Rett syndrome
Variation info
Gene MECP2
CLNDBN not specified Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296761G>C
CLNSRC
CLNACC RCV000133149.2, RCV000192592.1,