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rs587783547

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783547(A;A)
Make rs587783547(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401315
GeneDCX
is asnp
is mentioned by
dbSNPrs587783547
dbSNP (old)rs587783547
ClinGenrs587783547
ebirs587783547
HLIrs587783547
Exacrs587783547
Gnomadrs587783547
Varsomers587783547
Maprs587783547
PheGenIrs587783547
Biobankrs587783547
1000 genomesrs587783547
hgdprs587783547
ensemblrs587783547
gopubmedrs587783547
geneviewrs587783547
scholarrs587783547
googlers587783547
pharmgkbrs587783547
gwascentralrs587783547
openSNPrs587783547
23andMers587783547
23andMe allrs587783547
SNP Nexus

SNPshotrs587783547
SNPdbers587783547
MSV3drs587783547
GWAS Ctlgrs587783547
Max Magnitude0
ClinVar
Risk rs587783547(A;A)
Alt rs587783547(A;A)
Reference Rs587783547(G;G)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644543C>T
CLNSRC
CLNACC RCV000145841.1,