Have questions? Visit https://www.reddit.com/r/SNPedia

rs267608524

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608524(-;-)
Make rs267608524(-;AAAGCTGAGGCCGA)
Make rs267608524(AAAGCTGAGGCCGA;AAAGCTGAGGCCGA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031048
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608524
ebirs267608524
HLIrs267608524
Exacrs267608524
Varsomers267608524
Maprs267608524
PheGenIrs267608524
hapmaprs267608524
1000 genomesrs267608524
hgdprs267608524
ensemblrs267608524
gopubmedrs267608524
geneviewrs267608524
scholarrs267608524
googlers267608524
pharmgkbrs267608524
gwascentralrs267608524
openSNPrs267608524
23andMers267608524
23andMe allrs267608524
SNP Nexus

SNPshotrs267608524
SNPdbers267608524
MSV3drs267608524
GWAS Ctlgrs267608524
Max Magnitude0
ClinVar
Risk rs267608524(AAAGCTGAGGCCGA;AAAGCTGAGGCCGA)
Alt rs267608524(AAAGCTGAGGCCGA;AAAGCTGAGGCCGA)
Reference rs267608524(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296500_153296513dupTCGGCCTCAGCTTT
CLNSRC
CLNACC RCV000133235.2,