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rs587783092

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783092(-;-)
Make rs587783092(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030742
GeneMECP2
is asnp
is mentioned by
dbSNPrs587783092
ebirs587783092
HLIrs587783092
Exacrs587783092
Varsomers587783092
Maprs587783092
PheGenIrs587783092
hapmaprs587783092
1000 genomesrs587783092
hgdprs587783092
ensemblrs587783092
gopubmedrs587783092
geneviewrs587783092
scholarrs587783092
googlers587783092
pharmgkbrs587783092
gwascentralrs587783092
openSNPrs587783092
23andMers587783092
23andMe allrs587783092
SNP Nexus

SNPshotrs587783092
SNPdbers587783092
MSV3drs587783092
GWAS Ctlgrs587783092
Max Magnitude0
ClinVar
Risk rs587783092(;)
Alt rs587783092(;)
Reference rs587783092(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296193delG
CLNSRC
CLNACC RCV000144755.1,