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rs267608496

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs267608496(-;-)
Make rs267608496(-;TC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031284
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608496
ebirs267608496
HLIrs267608496
Exacrs267608496
Varsomers267608496
Maprs267608496
PheGenIrs267608496
hapmaprs267608496
1000 genomesrs267608496
hgdprs267608496
ensemblrs267608496
gopubmedrs267608496
geneviewrs267608496
scholarrs267608496
googlers267608496
pharmgkbrs267608496
gwascentralrs267608496
openSNPrs267608496
23andMers267608496
23andMe allrs267608496
SNP Nexus

SNPshotrs267608496
SNPdbers267608496
MSV3drs267608496
GWAS Ctlgrs267608496
Max Magnitude0
ClinVar
Risk rs267608496(;)
Alt rs267608496(;)
Reference rs267608496(TC;TC)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296735_153296736delGA
CLNSRC
CLNACC RCV000133157.2,