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rs797045519

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045519(-;TAGCC)
Make rs797045519(TAGCC;TAGCC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111410313
GeneDCX
is asnp
is mentioned by
dbSNPrs797045519
ClinGenrs797045519
ebirs797045519
HLIrs797045519
Exacrs797045519
Varsomers797045519
Maprs797045519
PheGenIrs797045519
hapmaprs797045519
1000 genomesrs797045519
hgdprs797045519
ensemblrs797045519
gopubmedrs797045519
geneviewrs797045519
scholarrs797045519
googlers797045519
pharmgkbrs797045519
gwascentralrs797045519
openSNPrs797045519
23andMers797045519
23andMe allrs797045519
SNP Nexus

SNPshotrs797045519
SNPdbers797045519
MSV3drs797045519
GWAS Ctlgrs797045519
Max Magnitude0
ClinVar
Risk rs797045519(TAGCC;TAGCC)
Alt rs797045519(TAGCC;TAGCC)
Reference Rs797045519(-;-)
Significance Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110653542_110653546dupGGCTA
CLNSRC
CLNACC RCV000193837.1,