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rs398122846

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122846(-;-)
Make rs398122846(-;C)
Make rs398122846(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70451973
GeneDLG3
is asnp
is mentioned by
dbSNPrs398122846
ebirs398122846
HLIrs398122846
Exacrs398122846
Varsomers398122846
Maprs398122846
PheGenIrs398122846
hapmaprs398122846
1000 genomesrs398122846
hgdprs398122846
ensemblrs398122846
gopubmedrs398122846
geneviewrs398122846
scholarrs398122846
googlers398122846
pharmgkbrs398122846
gwascentralrs398122846
openSNPrs398122846
23andMers398122846
23andMe allrs398122846
SNP Nexus

SNPshotrs398122846
SNPdbers398122846
MSV3drs398122846
GWAS Ctlgrs398122846
Max Magnitude0
ClinVar
Risk rs398122846(C;C)
Alt rs398122846(C;C)
Reference rs398122846(;)
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.69671823dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000022834.22,