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rs587783585

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783585(G;T)
Make rs587783585(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333108
GeneDCX
is asnp
is mentioned by
dbSNPrs587783585
ebirs587783585
HLIrs587783585
Exacrs587783585
Varsomers587783585
Maprs587783585
PheGenIrs587783585
hapmaprs587783585
1000 genomesrs587783585
hgdprs587783585
ensemblrs587783585
gopubmedrs587783585
geneviewrs587783585
scholarrs587783585
googlers587783585
pharmgkbrs587783585
gwascentralrs587783585
openSNPrs587783585
23andMers587783585
23andMe allrs587783585
SNP Nexus

SNPshotrs587783585
SNPdbers587783585
MSV3drs587783585
GWAS Ctlgrs587783585
Max Magnitude0
ClinVar
Risk rs587783585(T;T)
Alt rs587783585(T;T)
Reference rs587783585(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110576336C>A
CLNSRC
CLNACC RCV000145888.1,