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rs587783563

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783563(A;A)
Make rs587783563(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401138
GeneDCX
is asnp
is mentioned by
dbSNPrs587783563
ebirs587783563
HLIrs587783563
Exacrs587783563
Varsomers587783563
Maprs587783563
PheGenIrs587783563
hapmaprs587783563
1000 genomesrs587783563
hgdprs587783563
ensemblrs587783563
gopubmedrs587783563
geneviewrs587783563
scholarrs587783563
googlers587783563
pharmgkbrs587783563
gwascentralrs587783563
openSNPrs587783563
23andMers587783563
23andMe allrs587783563
SNP Nexus

SNPshotrs587783563
SNPdbers587783563
MSV3drs587783563
GWAS Ctlgrs587783563
Max Magnitude0
ClinVar
Risk rs587783563(A,T;A,T)
Alt rs587783563(A,T;A,T)
Reference rs587783563(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644366C>A; NC_000023.10:g.110644366C>T
CLNSRC
CLNACC RCV000145860.1, RCV000145859.1,