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rs796052225

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052225(G;T)
Make rs796052225(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41344318
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052225
ebirs796052225
HLIrs796052225
Exacrs796052225
Varsomers796052225
Maprs796052225
PheGenIrs796052225
hapmaprs796052225
1000 genomesrs796052225
hgdprs796052225
ensemblrs796052225
gopubmedrs796052225
geneviewrs796052225
scholarrs796052225
googlers796052225
pharmgkbrs796052225
gwascentralrs796052225
openSNPrs796052225
23andMers796052225
23andMe allrs796052225
SNP Nexus

SNPshotrs796052225
SNPdbers796052225
MSV3drs796052225
GWAS Ctlgrs796052225
Max Magnitude0
ClinVar
Risk rs796052225(T;T)
Alt rs796052225(T;T)
Reference rs796052225(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41203571G>T
CLNSRC
CLNACC RCV000190102.1,