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rs863223676

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223676(-;AG)
Make rs863223676(AG;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641151
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223676
dbSNP (classic)rs863223676
ClinGenrs863223676
ebirs863223676
HLIrs863223676
Exacrs863223676
Gnomadrs863223676
Varsomers863223676
LitVarrs863223676
Maprs863223676
PheGenIrs863223676
Biobankrs863223676
1000 genomesrs863223676
hgdprs863223676
ensemblrs863223676
geneviewrs863223676
scholarrs863223676
googlers863223676
pharmgkbrs863223676
gwascentralrs863223676
openSNPrs863223676
23andMers863223676
SNPshotrs863223676
SNPdbers863223676
MSV3drs863223676
GWAS Ctlgrs863223676
Max Magnitude0
ClinVar
Risk rs863223676(AG;AG)
Alt rs863223676(AG;AG)
Reference Rs863223676(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10621800_10621801dupCT
CLNSRC
CLNACC RCV000197674.1,