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rs61749707

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61749707(-;-)
Make rs61749707(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031274
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749707
ebirs61749707
HLIrs61749707
Exacrs61749707
Varsomers61749707
Maprs61749707
PheGenIrs61749707
hapmaprs61749707
1000 genomesrs61749707
hgdprs61749707
ensemblrs61749707
gopubmedrs61749707
geneviewrs61749707
scholarrs61749707
googlers61749707
pharmgkbrs61749707
gwascentralrs61749707
openSNPrs61749707
23andMers61749707
23andMe allrs61749707
SNP Nexus

SNPshotrs61749707
SNPdbers61749707
MSV3drs61749707
GWAS Ctlgrs61749707
Max Magnitude0
ClinVar
Risk rs61749707(;)
Alt rs61749707(;)
Reference rs61749707(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296725delC
CLNSRC
CLNACC RCV000133159.2,