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rs863223648

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223648(A;A)
Make rs863223648(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10663962
GeneJAG1, LOC105372526
is asnp
is mentioned by
dbSNPrs863223648
ebirs863223648
HLIrs863223648
Exacrs863223648
Varsomers863223648
Maprs863223648
PheGenIrs863223648
hapmaprs863223648
1000 genomesrs863223648
hgdprs863223648
ensemblrs863223648
gopubmedrs863223648
geneviewrs863223648
scholarrs863223648
googlers863223648
pharmgkbrs863223648
gwascentralrs863223648
openSNPrs863223648
23andMers863223648
23andMe allrs863223648
SNP Nexus

SNPshotrs863223648
SNPdbers863223648
MSV3drs863223648
GWAS Ctlgrs863223648
Max Magnitude0
ClinVar
Risk rs863223648(A;A)
Alt rs863223648(A;A)
Reference rs863223648(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10644610C>T
CLNSRC
CLNACC RCV000199991.2,