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rs61751361

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61751361(-;-)
Make rs61751361(-;A)
Make rs61751361(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030953
GeneMECP2
is asnp
is mentioned by
dbSNPrs61751361
ebirs61751361
HLIrs61751361
Exacrs61751361
Varsomers61751361
Maprs61751361
PheGenIrs61751361
hapmaprs61751361
1000 genomesrs61751361
hgdprs61751361
ensemblrs61751361
gopubmedrs61751361
geneviewrs61751361
scholarrs61751361
googlers61751361
pharmgkbrs61751361
gwascentralrs61751361
openSNPrs61751361
23andMers61751361
23andMe allrs61751361
SNP Nexus

SNPshotrs61751361
SNPdbers61751361
MSV3drs61751361
GWAS Ctlgrs61751361
Max Magnitude0
ClinVar
Risk rs61751361(A;A)
Alt rs61751361(A;A)
Reference rs61751361(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296404_153296405insT
CLNSRC
CLNACC RCV000133264.2,