Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783577

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783577(A;A)
Make rs587783577(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111401028
GeneDCX
is asnp
is mentioned by
dbSNPrs587783577
ebirs587783577
HLIrs587783577
Exacrs587783577
Varsomers587783577
Maprs587783577
PheGenIrs587783577
hapmaprs587783577
1000 genomesrs587783577
hgdprs587783577
ensemblrs587783577
gopubmedrs587783577
geneviewrs587783577
scholarrs587783577
googlers587783577
pharmgkbrs587783577
gwascentralrs587783577
openSNPrs587783577
23andMers587783577
23andMe allrs587783577
SNP Nexus

SNPshotrs587783577
SNPdbers587783577
MSV3drs587783577
GWAS Ctlgrs587783577
Max Magnitude0
ClinVar
Risk rs587783577(A;A)
Alt rs587783577(A;A)
Reference rs587783577(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110644256C>T
CLNSRC
CLNACC RCV000145880.1,