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rs587783523

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783523(G;T)
Make rs587783523(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410249
GeneDCX
is asnp
is mentioned by
dbSNPrs587783523
ebirs587783523
HLIrs587783523
Exacrs587783523
Varsomers587783523
Maprs587783523
PheGenIrs587783523
hapmaprs587783523
1000 genomesrs587783523
hgdprs587783523
ensemblrs587783523
gopubmedrs587783523
geneviewrs587783523
scholarrs587783523
googlers587783523
pharmgkbrs587783523
gwascentralrs587783523
openSNPrs587783523
23andMers587783523
23andMe allrs587783523
SNP Nexus

SNPshotrs587783523
SNPdbers587783523
MSV3drs587783523
GWAS Ctlgrs587783523
Max Magnitude0
ClinVar
Risk rs587783523(T;T)
Alt rs587783523(T;T)
Reference rs587783523(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653477C>A
CLNSRC
CLNACC RCV000145810.1,