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rs267608513

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608513(A;A)
Make rs267608513(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031155
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608513
ebirs267608513
HLIrs267608513
Exacrs267608513
Varsomers267608513
Maprs267608513
PheGenIrs267608513
hapmaprs267608513
1000 genomesrs267608513
hgdprs267608513
ensemblrs267608513
gopubmedrs267608513
geneviewrs267608513
scholarrs267608513
googlers267608513
pharmgkbrs267608513
gwascentralrs267608513
openSNPrs267608513
23andMers267608513
23andMe allrs267608513
SNP Nexus

SNPshotrs267608513
SNPdbers267608513
MSV3drs267608513
GWAS Ctlgrs267608513
Max Magnitude0
ClinVar
Risk rs267608513(A,G;A,G)
Alt rs267608513(A,G;A,G)
Reference rs267608513(C;C)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296606G>T
CLNSRC
CLNACC RCV000133192.2, RCV000193090.1,