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rs796052226

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052226(C;C)
Make rs796052226(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346548
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052226
ebirs796052226
HLIrs796052226
Exacrs796052226
Varsomers796052226
Maprs796052226
PheGenIrs796052226
hapmaprs796052226
1000 genomesrs796052226
hgdprs796052226
ensemblrs796052226
gopubmedrs796052226
geneviewrs796052226
scholarrs796052226
googlers796052226
pharmgkbrs796052226
gwascentralrs796052226
openSNPrs796052226
23andMers796052226
23andMe allrs796052226
SNP Nexus

SNPshotrs796052226
SNPdbers796052226
MSV3drs796052226
GWAS Ctlgrs796052226
Max Magnitude0
ClinVar
Risk rs796052226(C;C)
Alt rs796052226(C;C)
Reference rs796052226(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205801T>C
CLNSRC
CLNACC RCV000190103.1,