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rs61754427

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754427(-;-)
Make rs61754427(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032493
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754427
ebirs61754427
HLIrs61754427
Exacrs61754427
Varsomers61754427
Maprs61754427
PheGenIrs61754427
hapmaprs61754427
1000 genomesrs61754427
hgdprs61754427
ensemblrs61754427
gopubmedrs61754427
geneviewrs61754427
scholarrs61754427
googlers61754427
pharmgkbrs61754427
gwascentralrs61754427
openSNPrs61754427
23andMers61754427
23andMe allrs61754427
SNP Nexus

SNPshotrs61754427
SNPdbers61754427
MSV3drs61754427
GWAS Ctlgrs61754427
Max Magnitude0
ClinVar
Risk rs61754427(;)
Alt rs61754427(;)
Reference rs61754427(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297944delC
CLNSRC
CLNACC RCV000133292.2,