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rs61750259

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61750259(A;T)
Make rs61750259(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030963
GeneMECP2
is asnp
is mentioned by
dbSNPrs61750259
ebirs61750259
HLIrs61750259
Exacrs61750259
Varsomers61750259
Maprs61750259
PheGenIrs61750259
hapmaprs61750259
1000 genomesrs61750259
hgdprs61750259
ensemblrs61750259
gopubmedrs61750259
geneviewrs61750259
scholarrs61750259
googlers61750259
pharmgkbrs61750259
gwascentralrs61750259
openSNPrs61750259
23andMers61750259
23andMe allrs61750259
SNP Nexus

SNPshotrs61750259
SNPdbers61750259
MSV3drs61750259
GWAS Ctlgrs61750259
Max Magnitude0
ClinVar
Risk rs61750259(T;T)
Alt rs61750259(T;T)
Reference Rs61750259(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296414T>A
CLNSRC
CLNACC RCV000133260.2,