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rs267608550

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608550(A;G)
Make rs267608550(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position154030917
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608550
ebirs267608550
HLIrs267608550
Exacrs267608550
Varsomers267608550
Maprs267608550
PheGenIrs267608550
hapmaprs267608550
1000 genomesrs267608550
hgdprs267608550
ensemblrs267608550
gopubmedrs267608550
geneviewrs267608550
scholarrs267608550
googlers267608550
pharmgkbrs267608550
gwascentralrs267608550
openSNPrs267608550
23andMers267608550
23andMe allrs267608550
SNP Nexus

SNPshotrs267608550
SNPdbers267608550
MSV3drs267608550
GWAS Ctlgrs267608550
Max Magnitude0
ClinVar
Risk rs267608550(C,G;C,G)
Alt rs267608550(C,G;C,G)
Reference rs267608550(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MECP2
CLNDBN not specified
Reversed 1
HGVS NC_000023.10:g.153296368T>C
CLNSRC ClinVar GeneDx
CLNACC RCV000133287.3,