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rs863223678

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223678(C;T)
Make rs863223678(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10658618
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223678
ebirs863223678
HLIrs863223678
Exacrs863223678
Varsomers863223678
Maprs863223678
PheGenIrs863223678
hapmaprs863223678
1000 genomesrs863223678
hgdprs863223678
ensemblrs863223678
gopubmedrs863223678
geneviewrs863223678
scholarrs863223678
googlers863223678
pharmgkbrs863223678
gwascentralrs863223678
openSNPrs863223678
23andMers863223678
23andMe allrs863223678
SNP Nexus

SNPshotrs863223678
SNPdbers863223678
MSV3drs863223678
GWAS Ctlgrs863223678
Max Magnitude0
ClinVar
Risk rs863223678(T;T)
Alt rs863223678(T;T)
Reference rs863223678(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10639266G>A
CLNSRC
CLNACC RCV000195999.1,