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rs796052230

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs796052230(-;-)
Make rs796052230(-;AT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346542
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052230
ClinGenrs796052230
ebirs796052230
HLIrs796052230
Exacrs796052230
Varsomers796052230
Maprs796052230
PheGenIrs796052230
hapmaprs796052230
1000 genomesrs796052230
hgdprs796052230
ensemblrs796052230
gopubmedrs796052230
geneviewrs796052230
scholarrs796052230
googlers796052230
pharmgkbrs796052230
gwascentralrs796052230
openSNPrs796052230
23andMers796052230
23andMe allrs796052230
SNP Nexus

SNPshotrs796052230
SNPdbers796052230
MSV3drs796052230
GWAS Ctlgrs796052230
Max Magnitude0
ClinVar
Risk rs796052230(-;-)
Alt rs796052230(-;-)
Reference Rs796052230(AT;AT)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205795_41205796delAT
CLNSRC
CLNACC RCV000190107.1,