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rs61754456

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61754456(-;-)
Make rs61754456(-;A)
Make rs61754456(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032268
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754456
ebirs61754456
HLIrs61754456
Exacrs61754456
Varsomers61754456
Maprs61754456
PheGenIrs61754456
hapmaprs61754456
1000 genomesrs61754456
hgdprs61754456
ensemblrs61754456
gopubmedrs61754456
geneviewrs61754456
scholarrs61754456
googlers61754456
pharmgkbrs61754456
gwascentralrs61754456
openSNPrs61754456
23andMers61754456
23andMe allrs61754456
SNP Nexus

SNPshotrs61754456
SNPdbers61754456
MSV3drs61754456
GWAS Ctlgrs61754456
Max Magnitude0
ClinVar
Risk rs61754456(A;A)
Alt rs61754456(A;A)
Reference rs61754456(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297720dupT
CLNSRC
CLNACC RCV000133064.2,