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rs796052223

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052223(C;T)
Make rs796052223(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41343755
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052223
ebirs796052223
HLIrs796052223
Exacrs796052223
Varsomers796052223
Maprs796052223
PheGenIrs796052223
hapmaprs796052223
1000 genomesrs796052223
hgdprs796052223
ensemblrs796052223
gopubmedrs796052223
geneviewrs796052223
scholarrs796052223
googlers796052223
pharmgkbrs796052223
gwascentralrs796052223
openSNPrs796052223
23andMers796052223
23andMe allrs796052223
SNP Nexus

SNPshotrs796052223
SNPdbers796052223
MSV3drs796052223
GWAS Ctlgrs796052223
Max Magnitude0
ClinVar
Risk rs796052223(T;T)
Alt rs796052223(T;T)
Reference rs796052223(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41203008C>T
CLNSRC
CLNACC RCV000190100.2,