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rs587783553

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783553(A;G)
Make rs587783553(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401244
GeneDCX
is asnp
is mentioned by
dbSNPrs587783553
ebirs587783553
HLIrs587783553
Exacrs587783553
Varsomers587783553
Maprs587783553
PheGenIrs587783553
hapmaprs587783553
1000 genomesrs587783553
hgdprs587783553
ensemblrs587783553
gopubmedrs587783553
geneviewrs587783553
scholarrs587783553
googlers587783553
pharmgkbrs587783553
gwascentralrs587783553
openSNPrs587783553
23andMers587783553
23andMe allrs587783553
SNP Nexus

SNPshotrs587783553
SNPdbers587783553
MSV3drs587783553
GWAS Ctlgrs587783553
Max Magnitude0
ClinVar
Risk rs587783553(G,T;G,T)
Alt rs587783553(G,T;G,T)
Reference rs587783553(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644472T>A; NC_000023.10:g.110644472T>C
CLNSRC
CLNACC RCV000145848.1, RCV000145847.1,