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rs863223386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223386(-;-)
Make rs863223386(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position99467550
GeneVPS13B
is asnp
is mentioned by
dbSNPrs863223386
ClinGenrs863223386
ebirs863223386
HLIrs863223386
Exacrs863223386
Varsomers863223386
Maprs863223386
PheGenIrs863223386
hapmaprs863223386
1000 genomesrs863223386
hgdprs863223386
ensemblrs863223386
gopubmedrs863223386
geneviewrs863223386
scholarrs863223386
googlers863223386
pharmgkbrs863223386
gwascentralrs863223386
openSNPrs863223386
23andMers863223386
23andMe allrs863223386
SNP Nexus

SNPshotrs863223386
SNPdbers863223386
MSV3drs863223386
GWAS Ctlgrs863223386
Max Magnitude0
ClinVar
Risk rs863223386(-;-)
Alt rs863223386(-;-)
Reference Rs863223386(T;T)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene VPS13B
CLNDBN Abnormality of neuronal migration
Reversed 0
HGVS NC_000008.10:g.100479778delT
CLNSRC
CLNACC RCV000201400.1,