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rs587783568

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783568(A;A)
Make rs587783568(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401109
GeneDCX
is asnp
is mentioned by
dbSNPrs587783568
ebirs587783568
HLIrs587783568
Exacrs587783568
Varsomers587783568
Maprs587783568
PheGenIrs587783568
hapmaprs587783568
1000 genomesrs587783568
hgdprs587783568
ensemblrs587783568
gopubmedrs587783568
geneviewrs587783568
scholarrs587783568
googlers587783568
pharmgkbrs587783568
gwascentralrs587783568
openSNPrs587783568
23andMers587783568
23andMe allrs587783568
SNP Nexus

SNPshotrs587783568
SNPdbers587783568
MSV3drs587783568
GWAS Ctlgrs587783568
Max Magnitude0
ClinVar
Risk rs587783568(A,G,T;A,G,T)
Alt rs587783568(A,G,T;A,G,T)
Reference rs587783568(C;C)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644337G>A; NC_000023.10:g.110644337G>C; NC_000023.10:g.110644337G>T
CLNSRC
CLNACC RCV000145868.1, RCV000145867.1, RCV000145866.1,