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rs587783104

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783104(C;G)
Make rs587783104(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154030822
GeneMECP2
is asnp
is mentioned by
dbSNPrs587783104
ebirs587783104
HLIrs587783104
Exacrs587783104
Varsomers587783104
Maprs587783104
PheGenIrs587783104
hapmaprs587783104
1000 genomesrs587783104
hgdprs587783104
ensemblrs587783104
gopubmedrs587783104
geneviewrs587783104
scholarrs587783104
googlers587783104
pharmgkbrs587783104
gwascentralrs587783104
openSNPrs587783104
23andMers587783104
23andMe allrs587783104
SNP Nexus

SNPshotrs587783104
SNPdbers587783104
MSV3drs587783104
GWAS Ctlgrs587783104
Max Magnitude0
ClinVar
Risk rs587783104(G;G)
Alt rs587783104(G;G)
Reference rs587783104(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MECP2
CLNDBN not provided not specified
Reversed 1
HGVS NC_000023.10:g.153296273G>C
CLNSRC
CLNACC RCV000144771.3, RCV000235170.1,