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

rs267608521

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608521(C;TCAGGAAGCTT)
Make rs267608521(TCAGGAAGCTT;TCAGGAAGCTT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031078
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608521
ebirs267608521
HLIrs267608521
Exacrs267608521
Varsomers267608521
Maprs267608521
PheGenIrs267608521
hapmaprs267608521
1000 genomesrs267608521
hgdprs267608521
ensemblrs267608521
gopubmedrs267608521
geneviewrs267608521
scholarrs267608521
googlers267608521
pharmgkbrs267608521
gwascentralrs267608521
openSNPrs267608521
23andMers267608521
23andMe allrs267608521
SNP Nexus

SNPshotrs267608521
SNPdbers267608521
MSV3drs267608521
GWAS Ctlgrs267608521
Max Magnitude0
ClinVar
Risk rs267608521(TCAGGAAGCTT;TCAGGAAGCTT)
Alt rs267608521(TCAGGAAGCTT;TCAGGAAGCTT)
Reference rs267608521(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296529delGinsAAGCTTCCTGA
CLNSRC
CLNACC RCV000133224.2,