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rs875989802

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989802(A;A)
Make rs875989802(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41344278
GeneDDX3X
is asnp
is mentioned by
dbSNPrs875989802
ebirs875989802
HLIrs875989802
Exacrs875989802
Varsomers875989802
Maprs875989802
PheGenIrs875989802
hapmaprs875989802
1000 genomesrs875989802
hgdprs875989802
ensemblrs875989802
gopubmedrs875989802
geneviewrs875989802
scholarrs875989802
googlers875989802
pharmgkbrs875989802
gwascentralrs875989802
openSNPrs875989802
23andMers875989802
23andMe allrs875989802
SNP Nexus

SNPshotrs875989802
SNPdbers875989802
MSV3drs875989802
GWAS Ctlgrs875989802
Max Magnitude0
ClinVar
Risk rs875989802(A;A)
Alt rs875989802(A;A)
Reference rs875989802(G;G)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene DDX3X
CLNDBN Mental retardation, X-linked 102
Reversed 0
HGVS NC_000023.10:g.41203531G>A
CLNSRC
CLNACC RCV000211100.1,