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rs797045025

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045025(A;A)
Make rs797045025(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41344351
GeneDDX3X
is asnp
is mentioned by
dbSNPrs797045025
ebirs797045025
HLIrs797045025
Exacrs797045025
Varsomers797045025
Maprs797045025
PheGenIrs797045025
hapmaprs797045025
1000 genomesrs797045025
hgdprs797045025
ensemblrs797045025
gopubmedrs797045025
geneviewrs797045025
scholarrs797045025
googlers797045025
pharmgkbrs797045025
gwascentralrs797045025
openSNPrs797045025
23andMers797045025
23andMe allrs797045025
SNP Nexus

SNPshotrs797045025
SNPdbers797045025
MSV3drs797045025
GWAS Ctlgrs797045025
Max Magnitude0
ClinVar
Risk rs797045025(A;A)
Alt rs797045025(A;A)
Reference rs797045025(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41203604G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190552.2,