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rs1017583398

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41346520
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1017583398
dbSNP (old)rs1017583398
ClinGenrs1017583398
ebirs1017583398
HLIrs1017583398
Exacrs1017583398
Gnomadrs1017583398
Varsomers1017583398
Maprs1017583398
PheGenIrs1017583398
Biobankrs1017583398
1000 genomesrs1017583398
hgdprs1017583398
ensemblrs1017583398
gopubmedrs1017583398
geneviewrs1017583398
scholarrs1017583398
googlers1017583398
pharmgkbrs1017583398
gwascentralrs1017583398
openSNPrs1017583398
23andMers1017583398
23andMe allrs1017583398
SNPshotrs1017583398
SNPdbers1017583398
MSV3drs1017583398
GWAS Ctlgrs1017583398
Max Magnitude0
ClinVar
Risk rs1017583398(G;G)
Alt rs1017583398(G;G)
Reference Rs1017583398(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205773C>G
CLNSRC
CLNACC RCV000478952.1,