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rs267608570

From SNPedia

Orientationminus
Geno Mag Summary
(CAAAGGCCCCC;CAAAGGCCCCC) 0 common in clinvar
Make rs267608570(-;-)
Make rs267608570(-;CAAAGGCCCCC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030691
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608570
ebirs267608570
HLIrs267608570
Exacrs267608570
Varsomers267608570
Maprs267608570
PheGenIrs267608570
hapmaprs267608570
1000 genomesrs267608570
hgdprs267608570
ensemblrs267608570
gopubmedrs267608570
geneviewrs267608570
scholarrs267608570
googlers267608570
pharmgkbrs267608570
gwascentralrs267608570
openSNPrs267608570
23andMers267608570
23andMe allrs267608570
SNP Nexus

SNPshotrs267608570
SNPdbers267608570
MSV3drs267608570
GWAS Ctlgrs267608570
Max Magnitude0
ClinVar
Risk rs267608570(;)
Alt rs267608570(;)
Reference rs267608570(CAAAGGCCCCC;CAAAGGCCCCC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296142_153296152delGGGGGCCTTTG
CLNSRC
CLNACC RCV000132862.2,