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rs863223361

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223361(A;A)
Make rs863223361(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position101985963
GeneDYNC1H1
is asnp
is mentioned by
dbSNPrs863223361
ebirs863223361
HLIrs863223361
Exacrs863223361
Varsomers863223361
Maprs863223361
PheGenIrs863223361
hapmaprs863223361
1000 genomesrs863223361
hgdprs863223361
ensemblrs863223361
gopubmedrs863223361
geneviewrs863223361
scholarrs863223361
googlers863223361
pharmgkbrs863223361
gwascentralrs863223361
openSNPrs863223361
23andMers863223361
23andMe allrs863223361
SNP Nexus

SNPshotrs863223361
SNPdbers863223361
MSV3drs863223361
GWAS Ctlgrs863223361
Max Magnitude0
ClinVar
Risk rs863223361(A;A)
Alt rs863223361(A;A)
Reference rs863223361(G;G)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene DYNC1H1
CLNDBN Abnormality of neuronal migration
Reversed 0
HGVS NC_000014.8:g.102452300G>A
CLNSRC
CLNACC RCV000201421.1,