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rs61754438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754438(-;-)
Make rs61754438(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032383
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754438
ebirs61754438
HLIrs61754438
Exacrs61754438
Varsomers61754438
Maprs61754438
PheGenIrs61754438
hapmaprs61754438
1000 genomesrs61754438
hgdprs61754438
ensemblrs61754438
gopubmedrs61754438
geneviewrs61754438
scholarrs61754438
googlers61754438
pharmgkbrs61754438
gwascentralrs61754438
openSNPrs61754438
23andMers61754438
23andMe allrs61754438
SNP Nexus

SNPshotrs61754438
SNPdbers61754438
MSV3drs61754438
GWAS Ctlgrs61754438
Max Magnitude0
ClinVar
Risk rs61754438(;)
Alt rs61754438(;)
Reference rs61754438(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297834delC
CLNSRC
CLNACC RCV000133030.2,