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rs1064795387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position41346602
GeneDDX3X
is asnp
is mentioned by
dbSNPrs1064795387
dbSNP (old)rs1064795387
ClinGenrs1064795387
ebirs1064795387
HLIrs1064795387
Exacrs1064795387
Gnomadrs1064795387
Varsomers1064795387
LitVarrs1064795387
Maprs1064795387
PheGenIrs1064795387
Biobankrs1064795387
1000 genomesrs1064795387
hgdprs1064795387
ensemblrs1064795387
gopubmedrs1064795387
geneviewrs1064795387
scholarrs1064795387
googlers1064795387
pharmgkbrs1064795387
gwascentralrs1064795387
openSNPrs1064795387
23andMers1064795387
23andMe allrs1064795387
SNPshotrs1064795387
SNPdbers1064795387
MSV3drs1064795387
GWAS Ctlgrs1064795387
Max Magnitude0
ClinVar
Risk rs1064795387(T;T)
Alt rs1064795387(T;T)
Reference Rs1064795387(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DDX3X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41205855C>T
CLNSRC
CLNACC RCV000484531.1,