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rs61749736

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61749736(-;-)
Make rs61749736(-;A)
Make rs61749736(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031150
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749736
ebirs61749736
HLIrs61749736
Exacrs61749736
Varsomers61749736
Maprs61749736
PheGenIrs61749736
hapmaprs61749736
1000 genomesrs61749736
hgdprs61749736
ensemblrs61749736
gopubmedrs61749736
geneviewrs61749736
scholarrs61749736
googlers61749736
pharmgkbrs61749736
gwascentralrs61749736
openSNPrs61749736
23andMers61749736
23andMe allrs61749736
SNP Nexus

SNPshotrs61749736
SNPdbers61749736
MSV3drs61749736
GWAS Ctlgrs61749736
Max Magnitude0
ClinVar
Risk rs61749736(A;A)
Alt rs61749736(A;A)
Reference rs61749736(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296601_153296602insT
CLNSRC
CLNACC RCV000133196.2,