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rs863223388

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223388(G;G)
Make rs863223388(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position103491969
GeneLOC101927870, RELN
is asnp
is mentioned by
dbSNPrs863223388
ebirs863223388
HLIrs863223388
Exacrs863223388
Varsomers863223388
Maprs863223388
PheGenIrs863223388
hapmaprs863223388
1000 genomesrs863223388
hgdprs863223388
ensemblrs863223388
gopubmedrs863223388
geneviewrs863223388
scholarrs863223388
googlers863223388
pharmgkbrs863223388
gwascentralrs863223388
openSNPrs863223388
23andMers863223388
23andMe allrs863223388
SNP Nexus

SNPshotrs863223388
SNPdbers863223388
MSV3drs863223388
GWAS Ctlgrs863223388
Max Magnitude0
ClinVar
Risk rs863223388(G;G)
Alt rs863223388(G;G)
Reference rs863223388(T;T)
Significance Pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene LOC101927870 RELN
CLNDBN Abnormality of neuronal migration
Reversed 1
HGVS NC_000007.13:g.103132416A>C
CLNSRC
CLNACC RCV000201320.1,