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rs62952161

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62952161(-;-)
Make rs62952161(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031389
GeneMECP2
is asnp
is mentioned by
dbSNPrs62952161
ebirs62952161
HLIrs62952161
Exacrs62952161
Varsomers62952161
Maprs62952161
PheGenIrs62952161
hapmaprs62952161
1000 genomesrs62952161
hgdprs62952161
ensemblrs62952161
gopubmedrs62952161
geneviewrs62952161
scholarrs62952161
googlers62952161
pharmgkbrs62952161
gwascentralrs62952161
openSNPrs62952161
23andMers62952161
23andMe allrs62952161
SNP Nexus

SNPshotrs62952161
SNPdbers62952161
MSV3drs62952161
GWAS Ctlgrs62952161
Max Magnitude0
ClinVar
Risk rs62952161(;)
Alt rs62952161(;)
Reference rs62952161(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296840delC
CLNSRC
CLNACC RCV000133112.2,