Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223669

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs863223669(-;-)
Make rs863223669(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10652162
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223669
dbSNP (classic)rs863223669
ClinGenrs863223669
ebirs863223669
HLIrs863223669
Exacrs863223669
Gnomadrs863223669
Varsomers863223669
LitVarrs863223669
Maprs863223669
PheGenIrs863223669
Biobankrs863223669
1000 genomesrs863223669
hgdprs863223669
ensemblrs863223669
geneviewrs863223669
scholarrs863223669
googlers863223669
pharmgkbrs863223669
gwascentralrs863223669
openSNPrs863223669
23andMers863223669
SNPshotrs863223669
SNPdbers863223669
MSV3drs863223669
GWAS Ctlgrs863223669
Max Magnitude0
ClinVar
Risk rs863223669(-;-)
Alt rs863223669(-;-)
Reference Rs863223669(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10632810_10632811delAG
CLNSRC
CLNACC RCV000197305.1,