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rs587783579

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783579(-;-)
Make rs587783579(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401014
GeneDCX
is asnp
is mentioned by
dbSNPrs587783579
ebirs587783579
HLIrs587783579
Exacrs587783579
Varsomers587783579
Maprs587783579
PheGenIrs587783579
hapmaprs587783579
1000 genomesrs587783579
hgdprs587783579
ensemblrs587783579
gopubmedrs587783579
geneviewrs587783579
scholarrs587783579
googlers587783579
pharmgkbrs587783579
gwascentralrs587783579
openSNPrs587783579
23andMers587783579
23andMe allrs587783579
SNP Nexus

SNPshotrs587783579
SNPdbers587783579
MSV3drs587783579
GWAS Ctlgrs587783579
Max Magnitude0
ClinVar
Risk rs587783579(;)
Alt rs587783579(;)
Reference rs587783579(A;A)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644242delT
CLNSRC
CLNACC RCV000145882.1,