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rs63583161

From SNPedia

Orientationminus
Geno Mag Summary
(GCCCCCACCT;GCCCCCACCT) 0 common in clinvar
Make rs63583161(-;-)
Make rs63583161(-;GCCCCCACCT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030661
GeneMECP2
is asnp
is mentioned by
dbSNPrs63583161
ebirs63583161
HLIrs63583161
Exacrs63583161
Varsomers63583161
Maprs63583161
PheGenIrs63583161
hapmaprs63583161
1000 genomesrs63583161
hgdprs63583161
ensemblrs63583161
gopubmedrs63583161
geneviewrs63583161
scholarrs63583161
googlers63583161
pharmgkbrs63583161
gwascentralrs63583161
openSNPrs63583161
23andMers63583161
23andMe allrs63583161
SNP Nexus

SNPshotrs63583161
SNPdbers63583161
MSV3drs63583161
GWAS Ctlgrs63583161
Max Magnitude0
ClinVar
Risk rs63583161(;)
Alt rs63583161(;)
Reference rs63583161(GCCCCCACCT;GCCCCCACCT)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296112_153296121delAGGTGGGGGC
CLNSRC
CLNACC RCV000132898.2,