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rs587783532

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783532(A;A)
Make rs587783532(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410189
GeneDCX
is asnp
is mentioned by
dbSNPrs587783532
ebirs587783532
HLIrs587783532
Exacrs587783532
Varsomers587783532
Maprs587783532
PheGenIrs587783532
hapmaprs587783532
1000 genomesrs587783532
hgdprs587783532
ensemblrs587783532
gopubmedrs587783532
geneviewrs587783532
scholarrs587783532
googlers587783532
pharmgkbrs587783532
gwascentralrs587783532
openSNPrs587783532
23andMers587783532
23andMe allrs587783532
SNP Nexus

SNPshotrs587783532
SNPdbers587783532
MSV3drs587783532
GWAS Ctlgrs587783532
Max Magnitude0
ClinVar
Risk rs587783532(A;A)
Alt rs587783532(A;A)
Reference rs587783532(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653417G>T
CLNSRC
CLNACC RCV000145820.1,