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rs796052233

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052233(A;C)
Make rs796052233(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41345483
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052233
ebirs796052233
HLIrs796052233
Exacrs796052233
Varsomers796052233
Maprs796052233
PheGenIrs796052233
hapmaprs796052233
1000 genomesrs796052233
hgdprs796052233
ensemblrs796052233
gopubmedrs796052233
geneviewrs796052233
scholarrs796052233
googlers796052233
pharmgkbrs796052233
gwascentralrs796052233
openSNPrs796052233
23andMers796052233
23andMe allrs796052233
SNP Nexus

SNPshotrs796052233
SNPdbers796052233
MSV3drs796052233
GWAS Ctlgrs796052233
Max Magnitude0
ClinVar
Risk rs796052233(C;C)
Alt rs796052233(C;C)
Reference rs796052233(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41204736A>C
CLNSRC
CLNACC RCV000190110.2,