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rs797045515

From SNPedia

Orientationminus
Make rs797045515(-;-)
Make rs797045515(-;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111401169
GeneDCX
is asnp
is mentioned by
dbSNPrs797045515
ebirs797045515
HLIrs797045515
Exacrs797045515
Varsomers797045515
Maprs797045515
PheGenIrs797045515
hapmaprs797045515
1000 genomesrs797045515
hgdprs797045515
ensemblrs797045515
gopubmedrs797045515
geneviewrs797045515
scholarrs797045515
googlers797045515
pharmgkbrs797045515
gwascentralrs797045515
openSNPrs797045515
23andMers797045515
23andMe allrs797045515
SNP Nexus

SNPshotrs797045515
SNPdbers797045515
MSV3drs797045515
GWAS Ctlgrs797045515
Max Magnitude
ClinVar
Risk rs797045515(;)
Alt rs797045515(;)
Reference rs797045515(T;T)
Significance Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110644397delA
CLNSRC
CLNACC RCV000192741.1,