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rs1057523822

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523822(A;A)
Make rs1057523822(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41345459
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1057523822
dbSNP (old)rs1057523822
ClinGenrs1057523822
ebirs1057523822
HLIrs1057523822
Exacrs1057523822
Gnomadrs1057523822
Varsomers1057523822
Maprs1057523822
PheGenIrs1057523822
Biobankrs1057523822
1000 genomesrs1057523822
hgdprs1057523822
ensemblrs1057523822
gopubmedrs1057523822
geneviewrs1057523822
scholarrs1057523822
googlers1057523822
pharmgkbrs1057523822
gwascentralrs1057523822
openSNPrs1057523822
23andMers1057523822
23andMe allrs1057523822
SNPshotrs1057523822
SNPdbers1057523822
MSV3drs1057523822
GWAS Ctlgrs1057523822
Max Magnitude0
ClinVar
Risk rs1057523822(A;A)
Alt rs1057523822(A;A)
Reference Rs1057523822(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41204712G>A
CLNSRC
CLNACC RCV000433202.1,