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rs863223662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223662(-;T)
Make rs863223662(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10673523
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223662
dbSNP (old)rs863223662
ClinGenrs863223662
ebirs863223662
HLIrs863223662
Exacrs863223662
Gnomadrs863223662
Varsomers863223662
Maprs863223662
PheGenIrs863223662
Biobankrs863223662
1000 genomesrs863223662
hgdprs863223662
ensemblrs863223662
gopubmedrs863223662
geneviewrs863223662
scholarrs863223662
googlers863223662
pharmgkbrs863223662
gwascentralrs863223662
openSNPrs863223662
23andMers863223662
23andMe allrs863223662
SNP Nexus

SNPshotrs863223662
SNPdbers863223662
MSV3drs863223662
GWAS Ctlgrs863223662
Max Magnitude0
ClinVar
Risk rs863223662(T;T)
Alt rs863223662(T;T)
Reference Rs863223662(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10654172dupA
CLNSRC
CLNACC RCV000200125.1,