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rs796052231

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052231(C;T)
Make rs796052231(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41345280
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052231
ebirs796052231
HLIrs796052231
Exacrs796052231
Varsomers796052231
Maprs796052231
PheGenIrs796052231
hapmaprs796052231
1000 genomesrs796052231
hgdprs796052231
ensemblrs796052231
gopubmedrs796052231
geneviewrs796052231
scholarrs796052231
googlers796052231
pharmgkbrs796052231
gwascentralrs796052231
openSNPrs796052231
23andMers796052231
23andMe allrs796052231
SNP Nexus

SNPshotrs796052231
SNPdbers796052231
MSV3drs796052231
GWAS Ctlgrs796052231
Max Magnitude0
ClinVar
Risk rs796052231(T;T)
Alt rs796052231(T;T)
Reference rs796052231(C;C)
Significance Pathogenic
Disease not provided Mental retardation
Variation info
Gene DDX3X
CLNDBN not provided Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41204533C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190108.2, RCV000190550.2,