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rs587783090

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783090(-;-)
Make rs587783090(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032309
GeneMECP2
is asnp
is mentioned by
dbSNPrs587783090
ebirs587783090
HLIrs587783090
Exacrs587783090
Varsomers587783090
Maprs587783090
PheGenIrs587783090
hapmaprs587783090
1000 genomesrs587783090
hgdprs587783090
ensemblrs587783090
gopubmedrs587783090
geneviewrs587783090
scholarrs587783090
googlers587783090
pharmgkbrs587783090
gwascentralrs587783090
openSNPrs587783090
23andMers587783090
23andMe allrs587783090
SNP Nexus

SNPshotrs587783090
SNPdbers587783090
MSV3drs587783090
GWAS Ctlgrs587783090
Max Magnitude0
ClinVar
Risk rs587783090(;)
Alt rs587783090(;)
Reference rs587783090(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153297760delC
CLNSRC
CLNACC RCV000144752.1,