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rs796052238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052238(-;-)
Make rs796052238(-;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41345443
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052238
dbSNP (classic)rs796052238
ClinGenrs796052238
ebirs796052238
HLIrs796052238
Exacrs796052238
Gnomadrs796052238
Varsomers796052238
LitVarrs796052238
Maprs796052238
PheGenIrs796052238
Biobankrs796052238
1000 genomesrs796052238
hgdprs796052238
ensemblrs796052238
geneviewrs796052238
scholarrs796052238
googlers796052238
pharmgkbrs796052238
gwascentralrs796052238
openSNPrs796052238
23andMers796052238
SNPshotrs796052238
SNPdbers796052238
MSV3drs796052238
GWAS Ctlgrs796052238
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs796052238(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41204696delG
CLNSRC
CLNACC RCV000190115.1,