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rs796052227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052227(-;-)
Make rs796052227(-;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346234
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052227
dbSNP (classic)rs796052227
ClinGenrs796052227
ebirs796052227
HLIrs796052227
Exacrs796052227
Gnomadrs796052227
Varsomers796052227
LitVarrs796052227
Maprs796052227
PheGenIrs796052227
Biobankrs796052227
1000 genomesrs796052227
hgdprs796052227
ensemblrs796052227
geneviewrs796052227
scholarrs796052227
googlers796052227
pharmgkbrs796052227
gwascentralrs796052227
openSNPrs796052227
23andMers796052227
SNPshotrs796052227
SNPdbers796052227
MSV3drs796052227
GWAS Ctlgrs796052227
Max Magnitude0
ClinVar
Risk rs796052227(-;-)
Alt rs796052227(-;-)
Reference Rs796052227(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205487delG
CLNSRC
CLNACC RCV000190104.1,