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rs796052232

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052232(C;C)
Make rs796052232(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position41345408
GeneDDX3X
is asnp
is mentioned by
dbSNPrs796052232
ebirs796052232
HLIrs796052232
Exacrs796052232
Varsomers796052232
Maprs796052232
PheGenIrs796052232
hapmaprs796052232
1000 genomesrs796052232
hgdprs796052232
ensemblrs796052232
gopubmedrs796052232
geneviewrs796052232
scholarrs796052232
googlers796052232
pharmgkbrs796052232
gwascentralrs796052232
openSNPrs796052232
23andMers796052232
23andMe allrs796052232
SNP Nexus

SNPshotrs796052232
SNPdbers796052232
MSV3drs796052232
GWAS Ctlgrs796052232
Max Magnitude0
ClinVar
Risk rs796052232(C;C)
Alt rs796052232(C;C)
Reference rs796052232(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41204661T>C
CLNSRC
CLNACC RCV000190109.2,