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rs267608526

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs267608526(-;-)
Make rs267608526(-;TC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031035
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608526
ebirs267608526
HLIrs267608526
Exacrs267608526
Varsomers267608526
Maprs267608526
PheGenIrs267608526
hapmaprs267608526
1000 genomesrs267608526
hgdprs267608526
ensemblrs267608526
gopubmedrs267608526
geneviewrs267608526
scholarrs267608526
googlers267608526
pharmgkbrs267608526
gwascentralrs267608526
openSNPrs267608526
23andMers267608526
23andMe allrs267608526
SNP Nexus

SNPshotrs267608526
SNPdbers267608526
MSV3drs267608526
GWAS Ctlgrs267608526
Max Magnitude0
ClinVar
Risk rs267608526(;)
Alt rs267608526(;)
Reference rs267608526(TC;TC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296486_153296487delGA
CLNSRC
CLNACC RCV000133238.2,