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rs587783538

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783538(A;A)
Make rs587783538(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410100
GeneDCX
is asnp
is mentioned by
dbSNPrs587783538
ebirs587783538
HLIrs587783538
Exacrs587783538
Varsomers587783538
Maprs587783538
PheGenIrs587783538
hapmaprs587783538
1000 genomesrs587783538
hgdprs587783538
ensemblrs587783538
gopubmedrs587783538
geneviewrs587783538
scholarrs587783538
googlers587783538
pharmgkbrs587783538
gwascentralrs587783538
openSNPrs587783538
23andMers587783538
23andMe allrs587783538
SNP Nexus

SNPshotrs587783538
SNPdbers587783538
MSV3drs587783538
GWAS Ctlgrs587783538
Max Magnitude0
ClinVar
Risk rs587783538(A,T;A,T)
Alt rs587783538(A,T;A,T)
Reference rs587783538(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653328C>A; NC_000023.10:g.110653328C>T
CLNSRC
CLNACC RCV000145830.1, RCV000145829.1,