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rs587783539

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783539(C;C)
Make rs587783539(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410397
GeneDCX
is asnp
is mentioned by
dbSNPrs587783539
ebirs587783539
HLIrs587783539
Exacrs587783539
Varsomers587783539
Maprs587783539
PheGenIrs587783539
hapmaprs587783539
1000 genomesrs587783539
hgdprs587783539
ensemblrs587783539
gopubmedrs587783539
geneviewrs587783539
scholarrs587783539
googlers587783539
pharmgkbrs587783539
gwascentralrs587783539
openSNPrs587783539
23andMers587783539
23andMe allrs587783539
SNP Nexus

SNPshotrs587783539
SNPdbers587783539
MSV3drs587783539
GWAS Ctlgrs587783539
Max Magnitude0
ClinVar
Risk rs587783539(C;C)
Alt rs587783539(C;C)
Reference rs587783539(T;T)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653625A>G
CLNSRC
CLNACC RCV000145831.1,