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rs875989803

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989803(G;T)
Make rs875989803(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41343249
GeneDDX3X
is asnp
is mentioned by
dbSNPrs875989803
ebirs875989803
HLIrs875989803
Exacrs875989803
Varsomers875989803
Maprs875989803
PheGenIrs875989803
hapmaprs875989803
1000 genomesrs875989803
hgdprs875989803
ensemblrs875989803
gopubmedrs875989803
geneviewrs875989803
scholarrs875989803
googlers875989803
pharmgkbrs875989803
gwascentralrs875989803
openSNPrs875989803
23andMers875989803
23andMe allrs875989803
SNP Nexus

SNPshotrs875989803
SNPdbers875989803
MSV3drs875989803
GWAS Ctlgrs875989803
Max Magnitude0
ClinVar
Risk rs875989803(T;T)
Alt rs875989803(T;T)
Reference rs875989803(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.41202502G>T
CLNSRC
CLNACC RCV000211113.1,