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rs587783556

From SNPedia

Orientationminus
Geno Mag Summary
(GCAACAGTGCA;GCAACAGTGCA) 0 common in clinvar
Make rs587783556(-;-)
Make rs587783556(-;GCAACAGTGCA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401191
GeneDCX
is asnp
is mentioned by
dbSNPrs587783556
ebirs587783556
HLIrs587783556
Exacrs587783556
Varsomers587783556
Maprs587783556
PheGenIrs587783556
hapmaprs587783556
1000 genomesrs587783556
hgdprs587783556
ensemblrs587783556
gopubmedrs587783556
geneviewrs587783556
scholarrs587783556
googlers587783556
pharmgkbrs587783556
gwascentralrs587783556
openSNPrs587783556
23andMers587783556
23andMe allrs587783556
SNP Nexus

SNPshotrs587783556
SNPdbers587783556
MSV3drs587783556
GWAS Ctlgrs587783556
Max Magnitude0
ClinVar
Risk rs587783556(;)
Alt rs587783556(;)
Reference rs587783556(GCAACAGTGCA;GCAACAGTGCA)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644419_110644429delTGCACTGTTGC
CLNSRC
CLNACC RCV000145851.1,