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rs796052228

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052228(-;A)
Make rs796052228(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346296
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052228
ClinGenrs796052228
ebirs796052228
HLIrs796052228
Exacrs796052228
Varsomers796052228
Maprs796052228
PheGenIrs796052228
hapmaprs796052228
1000 genomesrs796052228
hgdprs796052228
ensemblrs796052228
gopubmedrs796052228
geneviewrs796052228
scholarrs796052228
googlers796052228
pharmgkbrs796052228
gwascentralrs796052228
openSNPrs796052228
23andMers796052228
23andMe allrs796052228
SNP Nexus

SNPshotrs796052228
SNPdbers796052228
MSV3drs796052228
GWAS Ctlgrs796052228
Max Magnitude0
ClinVar
Risk rs796052228(A;A)
Alt rs796052228(A;A)
Reference Rs796052228(;)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205549dupA
CLNSRC
CLNACC RCV000190105.1,