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rs587777360

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777360(C;C)
Make rs587777360(C;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position70450784
GeneDLG3
is asnp
is mentioned by
dbSNPrs587777360
ebirs587777360
HLIrs587777360
Exacrs587777360
Varsomers587777360
Maprs587777360
PheGenIrs587777360
hapmaprs587777360
1000 genomesrs587777360
hgdprs587777360
ensemblrs587777360
gopubmedrs587777360
geneviewrs587777360
scholarrs587777360
googlers587777360
pharmgkbrs587777360
gwascentralrs587777360
openSNPrs587777360
23andMers587777360
23andMe allrs587777360
SNP Nexus

SNPshotrs587777360
SNPdbers587777360
MSV3drs587777360
GWAS Ctlgrs587777360
Max Magnitude0
ClinVar
Risk rs587777360(C;C)
Alt rs587777360(C;C)
Reference rs587777360(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.69670634G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000115023.2,