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rs797045513

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045513(-;TAC)
Make rs797045513(TAC;TAC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111410083
GeneDCX
is asnp
is mentioned by
dbSNPrs797045513
ClinGenrs797045513
ebirs797045513
HLIrs797045513
Exacrs797045513
Varsomers797045513
Maprs797045513
PheGenIrs797045513
hapmaprs797045513
1000 genomesrs797045513
hgdprs797045513
ensemblrs797045513
gopubmedrs797045513
geneviewrs797045513
scholarrs797045513
googlers797045513
pharmgkbrs797045513
gwascentralrs797045513
openSNPrs797045513
23andMers797045513
23andMe allrs797045513
SNP Nexus

SNPshotrs797045513
SNPdbers797045513
MSV3drs797045513
GWAS Ctlgrs797045513
Max Magnitude0
ClinVar
Risk rs797045513(TAC;TAC)
Alt rs797045513(TAC;TAC)
Reference Rs797045513(;)
Significance Probable-Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110653312_110653314dupGTA
CLNSRC
CLNACC RCV000193684.1,