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rs587783520

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783520(-;-)
Make rs587783520(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410275
GeneDCX
is asnp
is mentioned by
dbSNPrs587783520
ebirs587783520
HLIrs587783520
Exacrs587783520
Varsomers587783520
Maprs587783520
PheGenIrs587783520
hapmaprs587783520
1000 genomesrs587783520
hgdprs587783520
ensemblrs587783520
gopubmedrs587783520
geneviewrs587783520
scholarrs587783520
googlers587783520
pharmgkbrs587783520
gwascentralrs587783520
openSNPrs587783520
23andMers587783520
23andMe allrs587783520
SNP Nexus

SNPshotrs587783520
SNPdbers587783520
MSV3drs587783520
GWAS Ctlgrs587783520
Max Magnitude0
ClinVar
Risk rs587783520(;)
Alt rs587783520(;)
Reference rs587783520(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653503delT
CLNSRC
CLNACC RCV000145807.1,