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rs1085307919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position111333107
GeneDCX
is asnp
is mentioned by
dbSNPrs1085307919
dbSNP (old)rs1085307919
ClinGenrs1085307919
ebirs1085307919
HLIrs1085307919
Exacrs1085307919
Gnomadrs1085307919
Varsomers1085307919
Maprs1085307919
PheGenIrs1085307919
Biobankrs1085307919
1000 genomesrs1085307919
hgdprs1085307919
ensemblrs1085307919
gopubmedrs1085307919
geneviewrs1085307919
scholarrs1085307919
googlers1085307919
pharmgkbrs1085307919
gwascentralrs1085307919
openSNPrs1085307919
23andMers1085307919
23andMe allrs1085307919
SNPshotrs1085307919
SNPdbers1085307919
MSV3drs1085307919
GWAS Ctlgrs1085307919
Max Magnitude0
ClinVar
Risk rs1085307919(A;A)
Alt rs1085307919(A;A)
Reference Rs1085307919(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DCX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.110576335G>T
CLNSRC
CLNACC RCV000489609.1,