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rs796052234

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052234(C;T)
Make rs796052234(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346375
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052234
ebirs796052234
HLIrs796052234
Exacrs796052234
Varsomers796052234
Maprs796052234
PheGenIrs796052234
hapmaprs796052234
1000 genomesrs796052234
hgdprs796052234
ensemblrs796052234
gopubmedrs796052234
geneviewrs796052234
scholarrs796052234
googlers796052234
pharmgkbrs796052234
gwascentralrs796052234
openSNPrs796052234
23andMers796052234
23andMe allrs796052234
SNP Nexus

SNPshotrs796052234
SNPdbers796052234
MSV3drs796052234
GWAS Ctlgrs796052234
Max Magnitude0
ClinVar
Risk rs796052234(T;T)
Alt rs796052234(T;T)
Reference rs796052234(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205628C>T
CLNSRC
CLNACC RCV000190111.1,