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rs61751443

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61751443(G;T)
Make rs61751443(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030911
GeneMECP2
is asnp
is mentioned by
dbSNPrs61751443
ebirs61751443
HLIrs61751443
Exacrs61751443
Varsomers61751443
Maprs61751443
PheGenIrs61751443
hapmaprs61751443
1000 genomesrs61751443
hgdprs61751443
ensemblrs61751443
gopubmedrs61751443
geneviewrs61751443
scholarrs61751443
googlers61751443
pharmgkbrs61751443
gwascentralrs61751443
openSNPrs61751443
23andMers61751443
23andMe allrs61751443
SNP Nexus

SNPshotrs61751443
SNPdbers61751443
MSV3drs61751443
GWAS Ctlgrs61751443
Max Magnitude0
ClinVar
Risk rs61751443(A,T;A,T)
Alt rs61751443(A,T;A,T)
Reference rs61751443(G;G)
Significance Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296362C>A; NC_000023.10:g.153296362C>T
CLNSRC
CLNACC RCV000133291.1, RCV000133290.3,