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rs869312692

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312692(C;T)
Make rs869312692(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41343291
GeneDDX3X
is asnp
is mentioned by
dbSNPrs869312692
ebirs869312692
HLIrs869312692
Exacrs869312692
Varsomers869312692
Maprs869312692
PheGenIrs869312692
hapmaprs869312692
1000 genomesrs869312692
hgdprs869312692
ensemblrs869312692
gopubmedrs869312692
geneviewrs869312692
scholarrs869312692
googlers869312692
pharmgkbrs869312692
gwascentralrs869312692
openSNPrs869312692
23andMers869312692
23andMe allrs869312692
SNP Nexus

SNPshotrs869312692
SNPdbers869312692
MSV3drs869312692
GWAS Ctlgrs869312692
Max Magnitude0
ClinVar
Risk rs869312692(T;T)
Alt rs869312692(T;T)
Reference rs869312692(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41202544C>T
CLNSRC
CLNACC RCV000209890.1,