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rs796052237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052237(-;A)
Make rs796052237(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41343271
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052237
dbSNP (old)rs796052237
ClinGenrs796052237
ebirs796052237
HLIrs796052237
Exacrs796052237
Gnomadrs796052237
Varsomers796052237
Maprs796052237
PheGenIrs796052237
Biobankrs796052237
1000 genomesrs796052237
hgdprs796052237
ensemblrs796052237
gopubmedrs796052237
geneviewrs796052237
scholarrs796052237
googlers796052237
pharmgkbrs796052237
gwascentralrs796052237
openSNPrs796052237
23andMers796052237
23andMe allrs796052237
SNP Nexus

SNPshotrs796052237
SNPdbers796052237
MSV3drs796052237
GWAS Ctlgrs796052237
Max Magnitude0
ClinVar
Risk rs796052237(A;A)
Alt rs796052237(A;A)
Reference Rs796052237(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41202524dupA
CLNSRC
CLNACC RCV000190114.1,