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rs796052235

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052235(A;A)
Make rs796052235(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41346376
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052235
ebirs796052235
HLIrs796052235
Exacrs796052235
Varsomers796052235
Maprs796052235
PheGenIrs796052235
hapmaprs796052235
1000 genomesrs796052235
hgdprs796052235
ensemblrs796052235
gopubmedrs796052235
geneviewrs796052235
scholarrs796052235
googlers796052235
pharmgkbrs796052235
gwascentralrs796052235
openSNPrs796052235
23andMers796052235
23andMe allrs796052235
SNP Nexus

SNPshotrs796052235
SNPdbers796052235
MSV3drs796052235
GWAS Ctlgrs796052235
Max Magnitude0
ClinVar
Risk rs796052235(A;A)
Alt rs796052235(A;A)
Reference rs796052235(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205629G>A
CLNSRC
CLNACC RCV000190112.2,