Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057521603

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521603(C;T)
Make rs1057521603(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41344342
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1057521603
dbSNP (old)rs1057521603
ClinGenrs1057521603
ebirs1057521603
HLIrs1057521603
Exacrs1057521603
Gnomadrs1057521603
Varsomers1057521603
Maprs1057521603
PheGenIrs1057521603
Biobankrs1057521603
1000 genomesrs1057521603
hgdprs1057521603
ensemblrs1057521603
gopubmedrs1057521603
geneviewrs1057521603
scholarrs1057521603
googlers1057521603
pharmgkbrs1057521603
gwascentralrs1057521603
openSNPrs1057521603
23andMers1057521603
23andMe allrs1057521603
SNPshotrs1057521603
SNPdbers1057521603
MSV3drs1057521603
GWAS Ctlgrs1057521603
Max Magnitude0
ClinVar
Risk rs1057521603(T;T)
Alt rs1057521603(T;T)
Reference Rs1057521603(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41203595C>T
CLNSRC
CLNACC RCV000434513.1,