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rs587783593

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783593(A;A)
Make rs587783593(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410304
GeneDCX
is asnp
is mentioned by
dbSNPrs587783593
ebirs587783593
HLIrs587783593
Exacrs587783593
Varsomers587783593
Maprs587783593
PheGenIrs587783593
hapmaprs587783593
1000 genomesrs587783593
hgdprs587783593
ensemblrs587783593
gopubmedrs587783593
geneviewrs587783593
scholarrs587783593
googlers587783593
pharmgkbrs587783593
gwascentralrs587783593
openSNPrs587783593
23andMers587783593
23andMe allrs587783593
SNP Nexus

SNPshotrs587783593
SNPdbers587783593
MSV3drs587783593
GWAS Ctlgrs587783593
Max Magnitude0
ClinVar
Risk rs587783593(A;A)
Alt rs587783593(A;A)
Reference rs587783593(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653532C>T
CLNSRC
CLNACC RCV000145896.1,