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rs587783529

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783529(C;T)
Make rs587783529(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410212
GeneDCX
is asnp
is mentioned by
dbSNPrs587783529
ebirs587783529
HLIrs587783529
Exacrs587783529
Varsomers587783529
Maprs587783529
PheGenIrs587783529
hapmaprs587783529
1000 genomesrs587783529
hgdprs587783529
ensemblrs587783529
gopubmedrs587783529
geneviewrs587783529
scholarrs587783529
googlers587783529
pharmgkbrs587783529
gwascentralrs587783529
openSNPrs587783529
23andMers587783529
23andMe allrs587783529
SNP Nexus

SNPshotrs587783529
SNPdbers587783529
MSV3drs587783529
GWAS Ctlgrs587783529
Max Magnitude0
ClinVar
Risk rs587783529(T;T)
Alt rs587783529(T;T)
Reference rs587783529(C;C)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653440G>A
CLNSRC
CLNACC RCV000145817.1,