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rs797045510

From SNPedia

Orientationminus
Make rs797045510(-;-)
Make rs797045510(-;TT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position111410376
GeneDCX
is asnp
is mentioned by
dbSNPrs797045510
ebirs797045510
HLIrs797045510
Exacrs797045510
Varsomers797045510
Maprs797045510
PheGenIrs797045510
hapmaprs797045510
1000 genomesrs797045510
hgdprs797045510
ensemblrs797045510
gopubmedrs797045510
geneviewrs797045510
scholarrs797045510
googlers797045510
pharmgkbrs797045510
gwascentralrs797045510
openSNPrs797045510
23andMers797045510
23andMe allrs797045510
SNP Nexus

SNPshotrs797045510
SNPdbers797045510
MSV3drs797045510
GWAS Ctlgrs797045510
Max Magnitude
ClinVar
Risk rs797045510(;)
Alt rs797045510(;)
Reference rs797045510(TT;TT)
Significance Pathogenic
Disease Abnormal cortical gyration
Variation info
Gene DCX
CLNDBN Abnormal cortical gyration
Reversed 1
HGVS NC_000023.10:g.110653604_110653605delAA
CLNSRC
CLNACC RCV000193604.1,