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rs863223652

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223652(C;T)
Make rs863223652(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10649087
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223652
ebirs863223652
HLIrs863223652
Exacrs863223652
Varsomers863223652
Maprs863223652
PheGenIrs863223652
hapmaprs863223652
1000 genomesrs863223652
hgdprs863223652
ensemblrs863223652
gopubmedrs863223652
geneviewrs863223652
scholarrs863223652
googlers863223652
pharmgkbrs863223652
gwascentralrs863223652
openSNPrs863223652
23andMers863223652
23andMe allrs863223652
SNP Nexus

SNPshotrs863223652
SNPdbers863223652
MSV3drs863223652
GWAS Ctlgrs863223652
Max Magnitude0
ClinVar
Risk rs863223652(T;T)
Alt rs863223652(T;T)
Reference rs863223652(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10629735G>A
CLNSRC
CLNACC RCV000198194.1,