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rs797045512

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045512(A;G)
Make rs797045512(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111410119
GeneDCX
is asnp
is mentioned by
dbSNPrs797045512
ebirs797045512
HLIrs797045512
Exacrs797045512
Varsomers797045512
Maprs797045512
PheGenIrs797045512
hapmaprs797045512
1000 genomesrs797045512
hgdprs797045512
ensemblrs797045512
gopubmedrs797045512
geneviewrs797045512
scholarrs797045512
googlers797045512
pharmgkbrs797045512
gwascentralrs797045512
openSNPrs797045512
23andMers797045512
23andMe allrs797045512
SNP Nexus

SNPshotrs797045512
SNPdbers797045512
MSV3drs797045512
GWAS Ctlgrs797045512
Max Magnitude0
ClinVar
Risk rs797045512(G;G)
Alt rs797045512(G;G)
Reference rs797045512(A;A)
Significance Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110653347T>C
CLNSRC
CLNACC RCV000192850.1,