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

rs797045517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045517(-;A)
Make rs797045517(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111401013
GeneDCX
is asnp
is mentioned by
dbSNPrs797045517
dbSNP (old)rs797045517
ClinGenrs797045517
ebirs797045517
HLIrs797045517
Exacrs797045517
Gnomadrs797045517
Varsomers797045517
Maprs797045517
PheGenIrs797045517
Biobankrs797045517
1000 genomesrs797045517
hgdprs797045517
ensemblrs797045517
gopubmedrs797045517
geneviewrs797045517
scholarrs797045517
googlers797045517
pharmgkbrs797045517
gwascentralrs797045517
openSNPrs797045517
23andMers797045517
23andMe allrs797045517
SNP Nexus

SNPshotrs797045517
SNPdbers797045517
MSV3drs797045517
GWAS Ctlgrs797045517
Max Magnitude0
ClinVar
Risk rs797045517(A;A)
Alt rs797045517(A;A)
Reference Rs797045517(-;-)
Significance Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110644242dupT
CLNSRC
CLNACC RCV000195154.1,