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rs267608606

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267608606(-;-)
Make rs267608606(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030664
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608606
ebirs267608606
HLIrs267608606
Exacrs267608606
Varsomers267608606
Maprs267608606
PheGenIrs267608606
hapmaprs267608606
1000 genomesrs267608606
hgdprs267608606
ensemblrs267608606
gopubmedrs267608606
geneviewrs267608606
scholarrs267608606
googlers267608606
pharmgkbrs267608606
gwascentralrs267608606
openSNPrs267608606
23andMers267608606
23andMe allrs267608606
SNP Nexus

SNPshotrs267608606
SNPdbers267608606
MSV3drs267608606
GWAS Ctlgrs267608606
Max Magnitude0
ClinVar
Risk rs267608606(;)
Alt rs267608606(;)
Reference rs267608606(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296115delT
CLNSRC
CLNACC RCV000132934.2,