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rs587783573

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783573(G;T)
Make rs587783573(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401067
GeneDCX
is asnp
is mentioned by
dbSNPrs587783573
ebirs587783573
HLIrs587783573
Exacrs587783573
Varsomers587783573
Maprs587783573
PheGenIrs587783573
hapmaprs587783573
1000 genomesrs587783573
hgdprs587783573
ensemblrs587783573
gopubmedrs587783573
geneviewrs587783573
scholarrs587783573
googlers587783573
pharmgkbrs587783573
gwascentralrs587783573
openSNPrs587783573
23andMers587783573
23andMe allrs587783573
SNP Nexus

SNPshotrs587783573
SNPdbers587783573
MSV3drs587783573
GWAS Ctlgrs587783573
Max Magnitude0
ClinVar
Risk rs587783573(T;T)
Alt rs587783573(T;T)
Reference rs587783573(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644295C>A
CLNSRC
CLNACC RCV000145876.1,