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rs863223656

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223656(C;T)
Make rs863223656(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641678
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223656
ebirs863223656
HLIrs863223656
Exacrs863223656
Varsomers863223656
Maprs863223656
PheGenIrs863223656
hapmaprs863223656
1000 genomesrs863223656
hgdprs863223656
ensemblrs863223656
gopubmedrs863223656
geneviewrs863223656
scholarrs863223656
googlers863223656
pharmgkbrs863223656
gwascentralrs863223656
openSNPrs863223656
23andMers863223656
23andMe allrs863223656
SNP Nexus

SNPshotrs863223656
SNPdbers863223656
MSV3drs863223656
GWAS Ctlgrs863223656
Max Magnitude0
ClinVar
Risk rs863223656(T;T)
Alt rs863223656(T;T)
Reference rs863223656(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10622326G>A
CLNSRC
CLNACC RCV000199200.1,