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

rs587783527

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783527(A;A)
Make rs587783527(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position111410217
GeneDCX
is asnp
is mentioned by
dbSNPrs587783527
ebirs587783527
HLIrs587783527
Exacrs587783527
Varsomers587783527
Maprs587783527
PheGenIrs587783527
hapmaprs587783527
1000 genomesrs587783527
hgdprs587783527
ensemblrs587783527
gopubmedrs587783527
geneviewrs587783527
scholarrs587783527
googlers587783527
pharmgkbrs587783527
gwascentralrs587783527
openSNPrs587783527
23andMers587783527
23andMe allrs587783527
SNP Nexus

SNPshotrs587783527
SNPdbers587783527
MSV3drs587783527
GWAS Ctlgrs587783527
Max Magnitude0
ClinVar
Risk rs587783527(A;A)
Alt rs587783527(A;A)
Reference rs587783527(G;G)
Significance Pathogenic
Disease Heterotopia
Variation info
Gene DCX
CLNDBN Heterotopia
Reversed 1
HGVS NC_000023.10:g.110653445C>T
CLNSRC
CLNACC RCV000145815.1,