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rs863223389

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223389(A;A)
Make rs863223389(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position103636325
GeneRELN
is asnp
is mentioned by
dbSNPrs863223389
ebirs863223389
HLIrs863223389
Exacrs863223389
Varsomers863223389
Maprs863223389
PheGenIrs863223389
hapmaprs863223389
1000 genomesrs863223389
hgdprs863223389
ensemblrs863223389
gopubmedrs863223389
geneviewrs863223389
scholarrs863223389
googlers863223389
pharmgkbrs863223389
gwascentralrs863223389
openSNPrs863223389
23andMers863223389
23andMe allrs863223389
SNP Nexus

SNPshotrs863223389
SNPdbers863223389
MSV3drs863223389
GWAS Ctlgrs863223389
Max Magnitude0
ClinVar
Risk rs863223389(A;A)
Alt rs863223389(A;A)
Reference rs863223389(G;G)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene RELN
CLNDBN Abnormality of neuronal migration
Reversed 1
HGVS NC_000007.13:g.103276772C>T
CLNSRC
CLNACC RCV000201320.1,