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rs61749709

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
Make rs61749709(-;A)
Make rs61749709(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031260
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749709
ebirs61749709
HLIrs61749709
Exacrs61749709
Varsomers61749709
Maprs61749709
PheGenIrs61749709
hapmaprs61749709
1000 genomesrs61749709
hgdprs61749709
ensemblrs61749709
gopubmedrs61749709
geneviewrs61749709
scholarrs61749709
googlers61749709
pharmgkbrs61749709
gwascentralrs61749709
openSNPrs61749709
23andMers61749709
23andMe allrs61749709
SNP Nexus

SNPshotrs61749709
SNPdbers61749709
MSV3drs61749709
GWAS Ctlgrs61749709
Max Magnitude0
ClinVar
Risk rs61749709(A;A)
Alt rs61749709(A;A)
Reference rs61749709(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296712dupT
CLNSRC
CLNACC RCV000133163.2,