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rs863223657

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223657(C;C)
Make rs863223657(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641644
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223657
ebirs863223657
HLIrs863223657
Exacrs863223657
Varsomers863223657
Maprs863223657
PheGenIrs863223657
hapmaprs863223657
1000 genomesrs863223657
hgdprs863223657
ensemblrs863223657
gopubmedrs863223657
geneviewrs863223657
scholarrs863223657
googlers863223657
pharmgkbrs863223657
gwascentralrs863223657
openSNPrs863223657
23andMers863223657
23andMe allrs863223657
SNP Nexus

SNPshotrs863223657
SNPdbers863223657
MSV3drs863223657
GWAS Ctlgrs863223657
Max Magnitude0
ClinVar
Risk rs863223657(C;C)
Alt rs863223657(C;C)
Reference rs863223657(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10622292C>G
CLNSRC
CLNACC RCV000195958.1,