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rs587783548

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783548(C;T)
Make rs587783548(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401309
GeneDCX
is asnp
is mentioned by
dbSNPrs587783548
ebirs587783548
HLIrs587783548
Exacrs587783548
Varsomers587783548
Maprs587783548
PheGenIrs587783548
hapmaprs587783548
1000 genomesrs587783548
hgdprs587783548
ensemblrs587783548
gopubmedrs587783548
geneviewrs587783548
scholarrs587783548
googlers587783548
pharmgkbrs587783548
gwascentralrs587783548
openSNPrs587783548
23andMers587783548
23andMe allrs587783548
SNP Nexus

SNPshotrs587783548
SNPdbers587783548
MSV3drs587783548
GWAS Ctlgrs587783548
Max Magnitude0
ClinVar
Risk rs587783548(T;T)
Alt rs587783548(T;T)
Reference rs587783548(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644537G>A
CLNSRC
CLNACC RCV000145842.1,