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rs863223377

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223377(C;C)
Make rs863223377(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position36090516
GeneWDR62
is asnp
is mentioned by
dbSNPrs863223377
ebirs863223377
HLIrs863223377
Exacrs863223377
Varsomers863223377
Maprs863223377
PheGenIrs863223377
hapmaprs863223377
1000 genomesrs863223377
hgdprs863223377
ensemblrs863223377
gopubmedrs863223377
geneviewrs863223377
scholarrs863223377
googlers863223377
pharmgkbrs863223377
gwascentralrs863223377
openSNPrs863223377
23andMers863223377
23andMe allrs863223377
SNP Nexus

SNPshotrs863223377
SNPdbers863223377
MSV3drs863223377
GWAS Ctlgrs863223377
Max Magnitude0
ClinVar
Risk rs863223377(C;C)
Alt rs863223377(C;C)
Reference rs863223377(T;T)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene WDR62
CLNDBN Abnormality of neuronal migration
Reversed 0
HGVS NC_000019.9:g.36581418T>C
CLNSRC
CLNACC RCV000201429.1,