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rs587783541

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783541(C;T)
Make rs587783541(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410095
GeneDCX
is asnp
is mentioned by
dbSNPrs587783541
ebirs587783541
HLIrs587783541
Exacrs587783541
Varsomers587783541
Maprs587783541
PheGenIrs587783541
hapmaprs587783541
1000 genomesrs587783541
hgdprs587783541
ensemblrs587783541
gopubmedrs587783541
geneviewrs587783541
scholarrs587783541
googlers587783541
pharmgkbrs587783541
gwascentralrs587783541
openSNPrs587783541
23andMers587783541
23andMe allrs587783541
SNP Nexus

SNPshotrs587783541
SNPdbers587783541
MSV3drs587783541
GWAS Ctlgrs587783541
Max Magnitude0
ClinVar
Risk rs587783541(T;T)
Alt rs587783541(T;T)
Reference rs587783541(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653323G>A
CLNSRC
CLNACC RCV000145833.1,