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rs1064793735

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position111410034
GeneDCX
is asnp
is mentioned by
dbSNPrs1064793735
dbSNP (old)rs1064793735
ClinGenrs1064793735
ebirs1064793735
HLIrs1064793735
Exacrs1064793735
Gnomadrs1064793735
Varsomers1064793735
LitVarrs1064793735
Maprs1064793735
PheGenIrs1064793735
Biobankrs1064793735
1000 genomesrs1064793735
hgdprs1064793735
ensemblrs1064793735
gopubmedrs1064793735
geneviewrs1064793735
scholarrs1064793735
googlers1064793735
pharmgkbrs1064793735
gwascentralrs1064793735
openSNPrs1064793735
23andMers1064793735
23andMe allrs1064793735
SNPshotrs1064793735
SNPdbers1064793735
MSV3drs1064793735
GWAS Ctlgrs1064793735
Max Magnitude0
ClinVar
Risk rs1064793735(-;-)
Alt rs1064793735(-;-)
Reference Rs1064793735(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DCX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.110653262delC
CLNSRC
CLNACC RCV000478400.1,