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rs1085307851

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
ChromosomeX
Position111410368
GeneDCX
is asnp
is mentioned by
dbSNPrs1085307851
dbSNP (old)rs1085307851
ClinGenrs1085307851
ebirs1085307851
HLIrs1085307851
Exacrs1085307851
Gnomadrs1085307851
Varsomers1085307851
Maprs1085307851
PheGenIrs1085307851
Biobankrs1085307851
1000 genomesrs1085307851
hgdprs1085307851
ensemblrs1085307851
gopubmedrs1085307851
geneviewrs1085307851
scholarrs1085307851
googlers1085307851
pharmgkbrs1085307851
gwascentralrs1085307851
openSNPrs1085307851
23andMers1085307851
23andMe allrs1085307851
SNPshotrs1085307851
SNPdbers1085307851
MSV3drs1085307851
GWAS Ctlgrs1085307851
Max Magnitude0
ClinVar
Risk rs1085307851(-;-)
Alt rs1085307851(-;-)
Reference Rs1085307851(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene DCX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.110653596_110653597delTT
CLNSRC
CLNACC RCV000489903.1,