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rs267606317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606317(C;T)
Make rs267606317(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position111410094
GeneDCX
is asnp
is mentioned by
dbSNPrs267606317
ebirs267606317
HLIrs267606317
Exacrs267606317
Varsomers267606317
Maprs267606317
PheGenIrs267606317
hapmaprs267606317
1000 genomesrs267606317
hgdprs267606317
ensemblrs267606317
gopubmedrs267606317
geneviewrs267606317
scholarrs267606317
googlers267606317
pharmgkbrs267606317
gwascentralrs267606317
openSNPrs267606317
23andMers267606317
23andMe allrs267606317
SNP Nexus

SNPshotrs267606317
SNPdbers267606317
MSV3drs267606317
GWAS Ctlgrs267606317
Max Magnitude0
ClinVar
Risk rs267606317(T;T)
Alt rs267606317(T;T)
Reference rs267606317(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 0
HGVS NC_000023.10:g.110653322C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000145834.1,