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rs267608639

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608639(-;-)
Make rs267608639(-;AG)
Make rs267608639(AG;AG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030374
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608639
ebirs267608639
HLIrs267608639
Exacrs267608639
Varsomers267608639
Maprs267608639
PheGenIrs267608639
hapmaprs267608639
1000 genomesrs267608639
hgdprs267608639
ensemblrs267608639
gopubmedrs267608639
geneviewrs267608639
scholarrs267608639
googlers267608639
pharmgkbrs267608639
gwascentralrs267608639
openSNPrs267608639
23andMers267608639
23andMe allrs267608639
SNP Nexus

SNPshotrs267608639
SNPdbers267608639
MSV3drs267608639
GWAS Ctlgrs267608639
Max Magnitude0
ClinVar
Risk rs267608639(AG;AG)
Alt rs267608639(AG;AG)
Reference rs267608639(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153295826_153295827dupCT
CLNSRC
CLNACC RCV000133015.2,