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rs587783537

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783537(G;G)
Make rs587783537(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410109
GeneDCX
is asnp
is mentioned by
dbSNPrs587783537
ebirs587783537
HLIrs587783537
Exacrs587783537
Varsomers587783537
Maprs587783537
PheGenIrs587783537
hapmaprs587783537
1000 genomesrs587783537
hgdprs587783537
ensemblrs587783537
gopubmedrs587783537
geneviewrs587783537
scholarrs587783537
googlers587783537
pharmgkbrs587783537
gwascentralrs587783537
openSNPrs587783537
23andMers587783537
23andMe allrs587783537
SNP Nexus

SNPshotrs587783537
SNPdbers587783537
MSV3drs587783537
GWAS Ctlgrs587783537
Max Magnitude0
ClinVar
Risk rs587783537(G;G)
Alt rs587783537(G;G)
Reference rs587783537(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653337A>C
CLNSRC
CLNACC RCV000145828.1,