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rs797045026

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045026(C;T)
Make rs797045026(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41345238
GeneDDX3X
is asnp
is mentioned by
dbSNPrs797045026
ebirs797045026
HLIrs797045026
Exacrs797045026
Varsomers797045026
Maprs797045026
PheGenIrs797045026
hapmaprs797045026
1000 genomesrs797045026
hgdprs797045026
ensemblrs797045026
gopubmedrs797045026
geneviewrs797045026
scholarrs797045026
googlers797045026
pharmgkbrs797045026
gwascentralrs797045026
openSNPrs797045026
23andMers797045026
23andMe allrs797045026
SNP Nexus

SNPshotrs797045026
SNPdbers797045026
MSV3drs797045026
GWAS Ctlgrs797045026
Max Magnitude0
ClinVar
Risk rs797045026(T;T)
Alt rs797045026(T;T)
Reference rs797045026(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41204491C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190554.2,