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rs61729440

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61729440(C;G)
Make rs61729440(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position111410133
GeneDCX
is asnp
is mentioned by
dbSNPrs61729440
ebirs61729440
HLIrs61729440
Exacrs61729440
Varsomers61729440
Maprs61729440
PheGenIrs61729440
hapmaprs61729440
1000 genomesrs61729440
hgdprs61729440
ensemblrs61729440
gopubmedrs61729440
geneviewrs61729440
scholarrs61729440
googlers61729440
pharmgkbrs61729440
gwascentralrs61729440
openSNPrs61729440
23andMers61729440
23andMe allrs61729440
SNP Nexus

SNPshotrs61729440
SNPdbers61729440
MSV3drs61729440
GWAS Ctlgrs61729440
Max Magnitude0
ClinVar
Risk rs61729440(G;G)
Alt rs61729440(G;G)
Reference rs61729440(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 0
HGVS NC_000023.10:g.110653361C>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000145826.1,