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rs796052224

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052224(C;C)
Make rs796052224(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41343761
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052224
ebirs796052224
HLIrs796052224
Exacrs796052224
Varsomers796052224
Maprs796052224
PheGenIrs796052224
hapmaprs796052224
1000 genomesrs796052224
hgdprs796052224
ensemblrs796052224
gopubmedrs796052224
geneviewrs796052224
scholarrs796052224
googlers796052224
pharmgkbrs796052224
gwascentralrs796052224
openSNPrs796052224
23andMers796052224
23andMe allrs796052224
SNP Nexus

SNPshotrs796052224
SNPdbers796052224
MSV3drs796052224
GWAS Ctlgrs796052224
Max Magnitude0
ClinVar
Risk rs796052224(C;C)
Alt rs796052224(C;C)
Reference rs796052224(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41203014T>C
CLNSRC
CLNACC RCV000190101.2,