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rs587783549

From SNPedia

Orientationminus
Geno Mag Summary
(AAC;AAC) 0 common in clinvar
Make rs587783549(-;-)
Make rs587783549(-;AAC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401302
GeneDCX
is asnp
is mentioned by
dbSNPrs587783549
ebirs587783549
HLIrs587783549
Exacrs587783549
Varsomers587783549
Maprs587783549
PheGenIrs587783549
hapmaprs587783549
1000 genomesrs587783549
hgdprs587783549
ensemblrs587783549
gopubmedrs587783549
geneviewrs587783549
scholarrs587783549
googlers587783549
pharmgkbrs587783549
gwascentralrs587783549
openSNPrs587783549
23andMers587783549
23andMe allrs587783549
SNP Nexus

SNPshotrs587783549
SNPdbers587783549
MSV3drs587783549
GWAS Ctlgrs587783549
Max Magnitude0
ClinVar
Risk rs587783549(;)
Alt rs587783549(;)
Reference rs587783549(AAC;AAC)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644530_110644532delGTT
CLNSRC
CLNACC RCV000145843.1,