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rs863223677

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223677(-;-)
Make rs863223677(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10640915
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223677
dbSNP (classic)rs863223677
ClinGenrs863223677
ebirs863223677
HLIrs863223677
Exacrs863223677
Gnomadrs863223677
Varsomers863223677
LitVarrs863223677
Maprs863223677
PheGenIrs863223677
Biobankrs863223677
1000 genomesrs863223677
hgdprs863223677
ensemblrs863223677
geneviewrs863223677
scholarrs863223677
googlers863223677
pharmgkbrs863223677
gwascentralrs863223677
openSNPrs863223677
23andMers863223677
SNPshotrs863223677
SNPdbers863223677
MSV3drs863223677
GWAS Ctlgrs863223677
Max Magnitude0
ClinVar
Risk rs863223677(-;-)
Alt rs863223677(-;-)
Reference Rs863223677(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10621563delC
CLNSRC
CLNACC RCV000199206.1,