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rs267608535

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608535(-;-)
Make rs267608535(-;G)
Make rs267608535(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030963
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608535
ebirs267608535
HLIrs267608535
Exacrs267608535
Varsomers267608535
Maprs267608535
PheGenIrs267608535
hapmaprs267608535
1000 genomesrs267608535
hgdprs267608535
ensemblrs267608535
gopubmedrs267608535
geneviewrs267608535
scholarrs267608535
googlers267608535
pharmgkbrs267608535
gwascentralrs267608535
openSNPrs267608535
23andMers267608535
23andMe allrs267608535
SNP Nexus

SNPshotrs267608535
SNPdbers267608535
MSV3drs267608535
GWAS Ctlgrs267608535
Max Magnitude0
ClinVar
Risk rs267608535(G;G)
Alt rs267608535(G;G)
Reference rs267608535(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296415dupC
CLNSRC
CLNACC RCV000133259.2,