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

rs61751367

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61751367(C;T)
Make rs61751367(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030939
GeneMECP2
is asnp
is mentioned by
dbSNPrs61751367
ebirs61751367
HLIrs61751367
Exacrs61751367
Varsomers61751367
Maprs61751367
PheGenIrs61751367
hapmaprs61751367
1000 genomesrs61751367
hgdprs61751367
ensemblrs61751367
gopubmedrs61751367
geneviewrs61751367
scholarrs61751367
googlers61751367
pharmgkbrs61751367
gwascentralrs61751367
openSNPrs61751367
23andMers61751367
23andMe allrs61751367
SNP Nexus

SNPshotrs61751367
SNPdbers61751367
MSV3drs61751367
GWAS Ctlgrs61751367
Max Magnitude0
ClinVar
Risk rs61751367(T;T)
Alt rs61751367(T;T)
Reference rs61751367(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296390G>A
CLNSRC
CLNACC RCV000133269.2,