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rs797045514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045514(-;C)
Make rs797045514(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111410059
GeneDCX
is asnp
is mentioned by
dbSNPrs797045514
dbSNP (old)rs797045514
ClinGenrs797045514
ebirs797045514
HLIrs797045514
Exacrs797045514
Gnomadrs797045514
Varsomers797045514
Maprs797045514
PheGenIrs797045514
Biobankrs797045514
1000 genomesrs797045514
hgdprs797045514
ensemblrs797045514
gopubmedrs797045514
geneviewrs797045514
scholarrs797045514
googlers797045514
pharmgkbrs797045514
gwascentralrs797045514
openSNPrs797045514
23andMers797045514
23andMe allrs797045514
SNP Nexus

SNPshotrs797045514
SNPdbers797045514
MSV3drs797045514
GWAS Ctlgrs797045514
Max Magnitude0
ClinVar
Risk rs797045514(C;C)
Alt rs797045514(C;C)
Reference Rs797045514(-;-)
Significance Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110653288dupG
CLNSRC
CLNACC RCV000194902.1,