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rs796052236

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052236(C;T)
Make rs796052236(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346403
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052236
ebirs796052236
HLIrs796052236
Exacrs796052236
Varsomers796052236
Maprs796052236
PheGenIrs796052236
hapmaprs796052236
1000 genomesrs796052236
hgdprs796052236
ensemblrs796052236
gopubmedrs796052236
geneviewrs796052236
scholarrs796052236
googlers796052236
pharmgkbrs796052236
gwascentralrs796052236
openSNPrs796052236
23andMers796052236
23andMe allrs796052236
SNP Nexus

SNPshotrs796052236
SNPdbers796052236
MSV3drs796052236
GWAS Ctlgrs796052236
Max Magnitude0
ClinVar
Risk rs796052236(T;T)
Alt rs796052236(T;T)
Reference rs796052236(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205656C>T
CLNSRC
CLNACC RCV000190113.1,