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rs587783528

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783528(A;G)
Make rs587783528(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410214
GeneDCX
is asnp
is mentioned by
dbSNPrs587783528
ebirs587783528
HLIrs587783528
Exacrs587783528
Varsomers587783528
Maprs587783528
PheGenIrs587783528
hapmaprs587783528
1000 genomesrs587783528
hgdprs587783528
ensemblrs587783528
gopubmedrs587783528
geneviewrs587783528
scholarrs587783528
googlers587783528
pharmgkbrs587783528
gwascentralrs587783528
openSNPrs587783528
23andMers587783528
23andMe allrs587783528
SNP Nexus

SNPshotrs587783528
SNPdbers587783528
MSV3drs587783528
GWAS Ctlgrs587783528
Max Magnitude0
ClinVar
Risk rs587783528(G;G)
Alt rs587783528(G;G)
Reference rs587783528(A;A)
Significance Probable-Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653442T>C
CLNSRC
CLNACC RCV000145816.1,