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rs61750256

From SNPedia

Orientationminus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs61750256(-;-)
Make rs61750256(-;AAAG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030969
GeneMECP2
is asnp
is mentioned by
dbSNPrs61750256
ebirs61750256
HLIrs61750256
Exacrs61750256
Varsomers61750256
Maprs61750256
PheGenIrs61750256
hapmaprs61750256
1000 genomesrs61750256
hgdprs61750256
ensemblrs61750256
gopubmedrs61750256
geneviewrs61750256
scholarrs61750256
googlers61750256
pharmgkbrs61750256
gwascentralrs61750256
openSNPrs61750256
23andMers61750256
23andMe allrs61750256
SNP Nexus

SNPshotrs61750256
SNPdbers61750256
MSV3drs61750256
GWAS Ctlgrs61750256
Max Magnitude0
ClinVar
Risk rs61750256(;)
Alt rs61750256(;)
Reference rs61750256(AAAG;AAAG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296420_153296423delCTTT
CLNSRC
CLNACC RCV000168696.2,