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rs61749702

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61749702(A;T)
Make rs61749702(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031299
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749702
ebirs61749702
HLIrs61749702
Exacrs61749702
Varsomers61749702
Maprs61749702
PheGenIrs61749702
hapmaprs61749702
1000 genomesrs61749702
hgdprs61749702
ensemblrs61749702
gopubmedrs61749702
geneviewrs61749702
scholarrs61749702
googlers61749702
pharmgkbrs61749702
gwascentralrs61749702
openSNPrs61749702
23andMers61749702
23andMe allrs61749702
SNP Nexus

SNPshotrs61749702
SNPdbers61749702
MSV3drs61749702
GWAS Ctlgrs61749702
Max Magnitude0
ClinVar
Risk rs61749702(G,T;G,T)
Alt rs61749702(G,T;G,T)
Reference rs61749702(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296750T>A
CLNSRC
CLNACC RCV000133153.2,