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rs587783567

From SNPedia

Orientationminus
Geno Mag Summary
(AGGCTGTG;AGGCTGTG) 0 common in clinvar
Make rs587783567(-;-)
Make rs587783567(-;AGGCTGTG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401110
GeneDCX
is asnp
is mentioned by
dbSNPrs587783567
ebirs587783567
HLIrs587783567
Exacrs587783567
Varsomers587783567
Maprs587783567
PheGenIrs587783567
hapmaprs587783567
1000 genomesrs587783567
hgdprs587783567
ensemblrs587783567
gopubmedrs587783567
geneviewrs587783567
scholarrs587783567
googlers587783567
pharmgkbrs587783567
gwascentralrs587783567
openSNPrs587783567
23andMers587783567
23andMe allrs587783567
SNP Nexus

SNPshotrs587783567
SNPdbers587783567
MSV3drs587783567
GWAS Ctlgrs587783567
Max Magnitude0
ClinVar
Risk rs587783567(;)
Alt rs587783567(;)
Reference rs587783567(AGGCTGTG;AGGCTGTG)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644338_110644345delCACAGCCT
CLNSRC
CLNACC RCV000145865.1,