Have questions? Visit https://www.reddit.com/r/SNPedia

rs61749703

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61749703(-;-)
Make rs61749703(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031297
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749703
ebirs61749703
HLIrs61749703
Exacrs61749703
Varsomers61749703
Maprs61749703
PheGenIrs61749703
hapmaprs61749703
1000 genomesrs61749703
hgdprs61749703
ensemblrs61749703
gopubmedrs61749703
geneviewrs61749703
scholarrs61749703
googlers61749703
pharmgkbrs61749703
gwascentralrs61749703
openSNPrs61749703
23andMers61749703
23andMe allrs61749703
SNP Nexus

SNPshotrs61749703
SNPdbers61749703
MSV3drs61749703
GWAS Ctlgrs61749703
Max Magnitude0
ClinVar
Risk rs61749703(;)
Alt rs61749703(;)
Reference rs61749703(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296748delT
CLNSRC
CLNACC RCV000133154.2,