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rs267608641

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608641(-;-)
Make rs267608641(-;TA)
Make rs267608641(TA;TA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030371
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608641
ebirs267608641
HLIrs267608641
Exacrs267608641
Varsomers267608641
Maprs267608641
PheGenIrs267608641
hapmaprs267608641
1000 genomesrs267608641
hgdprs267608641
ensemblrs267608641
gopubmedrs267608641
geneviewrs267608641
scholarrs267608641
googlers267608641
pharmgkbrs267608641
gwascentralrs267608641
openSNPrs267608641
23andMers267608641
23andMe allrs267608641
SNP Nexus

SNPshotrs267608641
SNPdbers267608641
MSV3drs267608641
GWAS Ctlgrs267608641
Max Magnitude0
ClinVar
Risk rs267608641(TA;TA)
Alt rs267608641(TA;TA)
Reference rs267608641(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153295823_153295824dupTA
CLNSRC
CLNACC RCV000133017.2,