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rs267608576

From SNPedia

Orientationminus
Geno Mag Summary
(ACCC;ACCC) 0 common in clinvar
Make rs267608576(-;-)
Make rs267608576(-;ACCC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030673
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608576
ebirs267608576
HLIrs267608576
Exacrs267608576
Varsomers267608576
Maprs267608576
PheGenIrs267608576
hapmaprs267608576
1000 genomesrs267608576
hgdprs267608576
ensemblrs267608576
gopubmedrs267608576
geneviewrs267608576
scholarrs267608576
googlers267608576
pharmgkbrs267608576
gwascentralrs267608576
openSNPrs267608576
23andMers267608576
23andMe allrs267608576
SNP Nexus

SNPshotrs267608576
SNPdbers267608576
MSV3drs267608576
GWAS Ctlgrs267608576
Max Magnitude0
ClinVar
Risk rs267608576(;)
Alt rs267608576(;)
Reference rs267608576(ACCC;ACCC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296124_153296127delGGGT
CLNSRC
CLNACC RCV000132879.2,