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rs587783561

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783561(A;A)
Make rs587783561(A;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401144
GeneDCX
is asnp
is mentioned by
dbSNPrs587783561
ebirs587783561
HLIrs587783561
Exacrs587783561
Varsomers587783561
Maprs587783561
PheGenIrs587783561
hapmaprs587783561
1000 genomesrs587783561
hgdprs587783561
ensemblrs587783561
gopubmedrs587783561
geneviewrs587783561
scholarrs587783561
googlers587783561
pharmgkbrs587783561
gwascentralrs587783561
openSNPrs587783561
23andMers587783561
23andMe allrs587783561
SNP Nexus

SNPshotrs587783561
SNPdbers587783561
MSV3drs587783561
GWAS Ctlgrs587783561
Max Magnitude0
ClinVar
Risk rs587783561(A;A)
Alt rs587783561(A;A)
Reference rs587783561(T;T)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644372A>T
CLNSRC
CLNACC RCV000145857.1,