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rs863223653

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223653(C;C)
Make rs863223653(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10645443
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223653
ebirs863223653
HLIrs863223653
Exacrs863223653
Varsomers863223653
Maprs863223653
PheGenIrs863223653
hapmaprs863223653
1000 genomesrs863223653
hgdprs863223653
ensemblrs863223653
gopubmedrs863223653
geneviewrs863223653
scholarrs863223653
googlers863223653
pharmgkbrs863223653
gwascentralrs863223653
openSNPrs863223653
23andMers863223653
23andMe allrs863223653
SNP Nexus

SNPshotrs863223653
SNPdbers863223653
MSV3drs863223653
GWAS Ctlgrs863223653
Max Magnitude0
ClinVar
Risk rs863223653(C;C)
Alt rs863223653(C;C)
Reference rs863223653(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10626091A>G
CLNSRC
CLNACC RCV000198719.1,