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rs61749741

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61749741(-;-)
Make rs61749741(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031132
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749741
ebirs61749741
HLIrs61749741
Exacrs61749741
Varsomers61749741
Maprs61749741
PheGenIrs61749741
hapmaprs61749741
1000 genomesrs61749741
hgdprs61749741
ensemblrs61749741
gopubmedrs61749741
geneviewrs61749741
scholarrs61749741
googlers61749741
pharmgkbrs61749741
gwascentralrs61749741
openSNPrs61749741
23andMers61749741
23andMe allrs61749741
SNP Nexus

SNPshotrs61749741
SNPdbers61749741
MSV3drs61749741
GWAS Ctlgrs61749741
Max Magnitude0
ClinVar
Risk rs61749741(;)
Alt rs61749741(;)
Reference rs61749741(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296583delG
CLNSRC
CLNACC RCV000133205.2,