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rs797045024

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045024(C;C)
Make rs797045024(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346527
GeneDDX3X
is asnp
is mentioned by
dbSNPrs797045024
ebirs797045024
HLIrs797045024
Exacrs797045024
Varsomers797045024
Maprs797045024
PheGenIrs797045024
hapmaprs797045024
1000 genomesrs797045024
hgdprs797045024
ensemblrs797045024
gopubmedrs797045024
geneviewrs797045024
scholarrs797045024
googlers797045024
pharmgkbrs797045024
gwascentralrs797045024
openSNPrs797045024
23andMers797045024
23andMe allrs797045024
SNP Nexus

SNPshotrs797045024
SNPdbers797045024
MSV3drs797045024
GWAS Ctlgrs797045024
Max Magnitude0
ClinVar
Risk rs797045024(C;C)
Alt rs797045024(C;C)
Reference rs797045024(T;T)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41205780T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000190551.2,