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rs587783136

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783136(A;T)
Make rs587783136(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031272
GeneMECP2
is asnp
is mentioned by
dbSNPrs587783136
ebirs587783136
HLIrs587783136
Exacrs587783136
Varsomers587783136
Maprs587783136
PheGenIrs587783136
hapmaprs587783136
1000 genomesrs587783136
hgdprs587783136
ensemblrs587783136
gopubmedrs587783136
geneviewrs587783136
scholarrs587783136
googlers587783136
pharmgkbrs587783136
gwascentralrs587783136
openSNPrs587783136
23andMers587783136
23andMe allrs587783136
SNP Nexus

SNPshotrs587783136
SNPdbers587783136
MSV3drs587783136
GWAS Ctlgrs587783136
Max Magnitude0
ClinVar
Risk rs587783136(T;T)
Alt rs587783136(T;T)
Reference rs587783136(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296723T>A
CLNSRC
CLNACC RCV000144809.2,