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rs587777359

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777359(C;C)
Make rs587777359(C;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position70445559
GeneDLG3
is asnp
is mentioned by
dbSNPrs587777359
ebirs587777359
HLIrs587777359
Exacrs587777359
Varsomers587777359
Maprs587777359
PheGenIrs587777359
hapmaprs587777359
1000 genomesrs587777359
hgdprs587777359
ensemblrs587777359
gopubmedrs587777359
geneviewrs587777359
scholarrs587777359
googlers587777359
pharmgkbrs587777359
gwascentralrs587777359
openSNPrs587777359
23andMers587777359
23andMe allrs587777359
SNP Nexus

SNPshotrs587777359
SNPdbers587777359
MSV3drs587777359
GWAS Ctlgrs587777359
Max Magnitude0
ClinVar
Risk rs587777359(C;C)
Alt rs587777359(C;C)
Reference rs587777359(G;G)
Significance Pathogenic
Disease X-Linked mental retardation 90
Variation info
Gene DLG3
CLNDBN X-Linked mental retardation 90
Reversed 0
HGVS NC_000023.10:g.69665409G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000115022.2,