Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783521

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783521(C;C)
Make rs587783521(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410271
GeneDCX
is asnp
is mentioned by
dbSNPrs587783521
ebirs587783521
HLIrs587783521
Exacrs587783521
Varsomers587783521
Maprs587783521
PheGenIrs587783521
hapmaprs587783521
1000 genomesrs587783521
hgdprs587783521
ensemblrs587783521
gopubmedrs587783521
geneviewrs587783521
scholarrs587783521
googlers587783521
pharmgkbrs587783521
gwascentralrs587783521
openSNPrs587783521
23andMers587783521
23andMe allrs587783521
SNP Nexus

SNPshotrs587783521
SNPdbers587783521
MSV3drs587783521
GWAS Ctlgrs587783521
Max Magnitude0
ClinVar
Risk rs587783521(C;C)
Alt rs587783521(C;C)
Reference rs587783521(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653499A>G
CLNSRC
CLNACC RCV000145808.1,