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rs587783580

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783580(C;C)
Make rs587783580(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401012
GeneDCX
is asnp
is mentioned by
dbSNPrs587783580
ebirs587783580
HLIrs587783580
Exacrs587783580
Varsomers587783580
Maprs587783580
PheGenIrs587783580
hapmaprs587783580
1000 genomesrs587783580
hgdprs587783580
ensemblrs587783580
gopubmedrs587783580
geneviewrs587783580
scholarrs587783580
googlers587783580
pharmgkbrs587783580
gwascentralrs587783580
openSNPrs587783580
23andMers587783580
23andMe allrs587783580
SNP Nexus

SNPshotrs587783580
SNPdbers587783580
MSV3drs587783580
GWAS Ctlgrs587783580
Max Magnitude0
ClinVar
Risk rs587783580(C;C)
Alt rs587783580(C;C)
Reference rs587783580(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644240A>G
CLNSRC
CLNACC RCV000145883.1,