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rs267608634

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs267608634(-;-)
Make rs267608634(-;AG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030412
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608634
ebirs267608634
HLIrs267608634
Exacrs267608634
Varsomers267608634
Maprs267608634
PheGenIrs267608634
hapmaprs267608634
1000 genomesrs267608634
hgdprs267608634
ensemblrs267608634
gopubmedrs267608634
geneviewrs267608634
scholarrs267608634
googlers267608634
pharmgkbrs267608634
gwascentralrs267608634
openSNPrs267608634
23andMers267608634
23andMe allrs267608634
SNP Nexus

SNPshotrs267608634
SNPdbers267608634
MSV3drs267608634
GWAS Ctlgrs267608634
Max Magnitude0
ClinVar
Risk rs267608634(;)
Alt rs267608634(;)
Reference rs267608634(AG;AG)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MECP2
CLNDBN Mental retardation, X-linked, syndromic 13
Reversed 1
HGVS NC_000023.10:g.153295863_153295864delCT
CLNSRC
CLNACC RCV000133004.2,