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rs61754430

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61754430(-;-)
Make rs61754430(-;G)
Make rs61754430(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032457
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754430
ebirs61754430
HLIrs61754430
Exacrs61754430
Varsomers61754430
Maprs61754430
PheGenIrs61754430
hapmaprs61754430
1000 genomesrs61754430
hgdprs61754430
ensemblrs61754430
gopubmedrs61754430
geneviewrs61754430
scholarrs61754430
googlers61754430
pharmgkbrs61754430
gwascentralrs61754430
openSNPrs61754430
23andMers61754430
23andMe allrs61754430
SNP Nexus

SNPshotrs61754430
SNPdbers61754430
MSV3drs61754430
GWAS Ctlgrs61754430
Max Magnitude0
ClinVar
Risk rs61754430(G;G)
Alt rs61754430(G;G)
Reference rs61754430(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297909dupC
CLNSRC
CLNACC RCV000132980.2,