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rs863223681

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223681(A;A)
Make rs863223681(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10644885
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223681
ebirs863223681
HLIrs863223681
Exacrs863223681
Varsomers863223681
Maprs863223681
PheGenIrs863223681
hapmaprs863223681
1000 genomesrs863223681
hgdprs863223681
ensemblrs863223681
gopubmedrs863223681
geneviewrs863223681
scholarrs863223681
googlers863223681
pharmgkbrs863223681
gwascentralrs863223681
openSNPrs863223681
23andMers863223681
23andMe allrs863223681
SNP Nexus

SNPshotrs863223681
SNPdbers863223681
MSV3drs863223681
GWAS Ctlgrs863223681
Max Magnitude0
ClinVar
Risk rs863223681(A;A)
Alt rs863223681(A;A)
Reference rs863223681(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10625533C>T
CLNSRC
CLNACC RCV000196444.1,