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rs863223667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223667(-;G)
Make rs863223667(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10672817
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223667
ClinGenrs863223667
ebirs863223667
HLIrs863223667
Exacrs863223667
Varsomers863223667
Maprs863223667
PheGenIrs863223667
hapmaprs863223667
1000 genomesrs863223667
hgdprs863223667
ensemblrs863223667
gopubmedrs863223667
geneviewrs863223667
scholarrs863223667
googlers863223667
pharmgkbrs863223667
gwascentralrs863223667
openSNPrs863223667
23andMers863223667
23andMe allrs863223667
SNP Nexus

SNPshotrs863223667
SNPdbers863223667
MSV3drs863223667
GWAS Ctlgrs863223667
Max Magnitude0
ClinVar
Risk rs863223667(G;G)
Alt rs863223667(G;G)
Reference Rs863223667(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10653466dupC
CLNSRC
CLNACC RCV000198317.1,