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rs267608624

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608624(-;-)
Make rs267608624(-;T)
Make rs267608624(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030507
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608624
ebirs267608624
HLIrs267608624
Exacrs267608624
Varsomers267608624
Maprs267608624
PheGenIrs267608624
hapmaprs267608624
1000 genomesrs267608624
hgdprs267608624
ensemblrs267608624
gopubmedrs267608624
geneviewrs267608624
scholarrs267608624
googlers267608624
pharmgkbrs267608624
gwascentralrs267608624
openSNPrs267608624
23andMers267608624
23andMe allrs267608624
SNP Nexus

SNPshotrs267608624
SNPdbers267608624
MSV3drs267608624
GWAS Ctlgrs267608624
Max Magnitude0
ClinVar
Risk rs267608624(T;T)
Alt rs267608624(T;T)
Reference rs267608624(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153295959dupA
CLNSRC
CLNACC RCV000132987.2,