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rs267608531

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608531(-;-)
Make rs267608531(-;A)
Make rs267608531(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030973
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608531
ebirs267608531
HLIrs267608531
Exacrs267608531
Varsomers267608531
Maprs267608531
PheGenIrs267608531
hapmaprs267608531
1000 genomesrs267608531
hgdprs267608531
ensemblrs267608531
gopubmedrs267608531
geneviewrs267608531
scholarrs267608531
googlers267608531
pharmgkbrs267608531
gwascentralrs267608531
openSNPrs267608531
23andMers267608531
23andMe allrs267608531
SNP Nexus

SNPshotrs267608531
SNPdbers267608531
MSV3drs267608531
GWAS Ctlgrs267608531
Max Magnitude0
ClinVar
Risk rs267608531(A;A)
Alt rs267608531(A;A)
Reference rs267608531(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296425dupT
CLNSRC
CLNACC RCV000133255.2,