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rs797045520

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045520(-;A)
Make rs797045520(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111330974
GeneDCX
is asnp
is mentioned by
dbSNPrs797045520
ClinGenrs797045520
ebirs797045520
HLIrs797045520
Exacrs797045520
Varsomers797045520
Maprs797045520
PheGenIrs797045520
hapmaprs797045520
1000 genomesrs797045520
hgdprs797045520
ensemblrs797045520
gopubmedrs797045520
geneviewrs797045520
scholarrs797045520
googlers797045520
pharmgkbrs797045520
gwascentralrs797045520
openSNPrs797045520
23andMers797045520
23andMe allrs797045520
SNP Nexus

SNPshotrs797045520
SNPdbers797045520
MSV3drs797045520
GWAS Ctlgrs797045520
Max Magnitude0
ClinVar
Risk rs797045520(A;A)
Alt rs797045520(A;A)
Reference Rs797045520(;)
Significance Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110574203dupT
CLNSRC
CLNACC RCV000193265.1,