Have questions? Visit https://www.reddit.com/r/SNPedia

rs398122847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122847(C;G)
Make rs398122847(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position70454284
GeneDLG3
is asnp
is mentioned by
dbSNPrs398122847
ebirs398122847
HLIrs398122847
Exacrs398122847
Varsomers398122847
Maprs398122847
PheGenIrs398122847
hapmaprs398122847
1000 genomesrs398122847
hgdprs398122847
ensemblrs398122847
gopubmedrs398122847
geneviewrs398122847
scholarrs398122847
googlers398122847
pharmgkbrs398122847
gwascentralrs398122847
openSNPrs398122847
23andMers398122847
23andMe allrs398122847
SNP Nexus

SNPshotrs398122847
SNPdbers398122847
MSV3drs398122847
GWAS Ctlgrs398122847
Max Magnitude0
ClinVar
Risk rs398122847(G;G)
Alt rs398122847(G;G)
Reference rs398122847(C;C)
Significance Pathogenic
Disease X-Linked mental retardation 90
Variation info
Gene DLG3-AS1 DLG3
CLNDBN X-Linked mental retardation 90
Reversed 0
HGVS NC_000023.10:g.69674134C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022835.24,