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rs1064794223

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position111401190
GeneDCX
is asnp
is mentioned by
dbSNPrs1064794223
dbSNP (old)rs1064794223
ClinGenrs1064794223
ebirs1064794223
HLIrs1064794223
Exacrs1064794223
Gnomadrs1064794223
Varsomers1064794223
Maprs1064794223
PheGenIrs1064794223
Biobankrs1064794223
1000 genomesrs1064794223
hgdprs1064794223
ensemblrs1064794223
gopubmedrs1064794223
geneviewrs1064794223
scholarrs1064794223
googlers1064794223
pharmgkbrs1064794223
gwascentralrs1064794223
openSNPrs1064794223
23andMers1064794223
23andMe allrs1064794223
SNPshotrs1064794223
SNPdbers1064794223
MSV3drs1064794223
GWAS Ctlgrs1064794223
Max Magnitude0
ClinVar
Risk rs1064794223(T;T)
Alt rs1064794223(T;T)
Reference Rs1064794223(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DCX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.110644418G>A
CLNSRC
CLNACC RCV000480025.1,