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rs869320681

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320681(A;A)
Make rs869320681(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41344247
GeneDDX3X
is asnp
is mentioned by
dbSNPrs869320681
ebirs869320681
HLIrs869320681
Exacrs869320681
Varsomers869320681
Maprs869320681
PheGenIrs869320681
hapmaprs869320681
1000 genomesrs869320681
hgdprs869320681
ensemblrs869320681
gopubmedrs869320681
geneviewrs869320681
scholarrs869320681
googlers869320681
pharmgkbrs869320681
gwascentralrs869320681
openSNPrs869320681
23andMers869320681
23andMe allrs869320681
SNP Nexus

SNPshotrs869320681
SNPdbers869320681
MSV3drs869320681
GWAS Ctlgrs869320681
Max Magnitude0
ClinVar
Risk rs869320681(A;A)
Alt rs869320681(A;A)
Reference rs869320681(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41203500C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190553.2,