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rs587783587

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783587(C;C)
Make rs587783587(C;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111333086
GeneDCX
is asnp
is mentioned by
dbSNPrs587783587
ebirs587783587
HLIrs587783587
Exacrs587783587
Varsomers587783587
Maprs587783587
PheGenIrs587783587
hapmaprs587783587
1000 genomesrs587783587
hgdprs587783587
ensemblrs587783587
gopubmedrs587783587
geneviewrs587783587
scholarrs587783587
googlers587783587
pharmgkbrs587783587
gwascentralrs587783587
openSNPrs587783587
23andMers587783587
23andMe allrs587783587
SNP Nexus

SNPshotrs587783587
SNPdbers587783587
MSV3drs587783587
GWAS Ctlgrs587783587
Max Magnitude0
ClinVar
Risk rs587783587(C;C)
Alt rs587783587(C;C)
Reference rs587783587(G;G)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110576314C>G
CLNSRC
CLNACC RCV000145890.1,