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rs267608503

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608503(-;-)
Make rs267608503(-;G)
Make rs267608503(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031226
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608503
ebirs267608503
HLIrs267608503
Exacrs267608503
Varsomers267608503
Maprs267608503
PheGenIrs267608503
hapmaprs267608503
1000 genomesrs267608503
hgdprs267608503
ensemblrs267608503
gopubmedrs267608503
geneviewrs267608503
scholarrs267608503
googlers267608503
pharmgkbrs267608503
gwascentralrs267608503
openSNPrs267608503
23andMers267608503
23andMe allrs267608503
SNP Nexus

SNPshotrs267608503
SNPdbers267608503
MSV3drs267608503
GWAS Ctlgrs267608503
Max Magnitude0
ClinVar
Risk rs267608503(G;G)
Alt rs267608503(G;G)
Reference rs267608503(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296678dupC
CLNSRC
CLNACC RCV000133172.2,