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rs863223660

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223660(A;G)
Make rs863223660(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10639957
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223660
ebirs863223660
HLIrs863223660
Exacrs863223660
Varsomers863223660
Maprs863223660
PheGenIrs863223660
hapmaprs863223660
1000 genomesrs863223660
hgdprs863223660
ensemblrs863223660
gopubmedrs863223660
geneviewrs863223660
scholarrs863223660
googlers863223660
pharmgkbrs863223660
gwascentralrs863223660
openSNPrs863223660
23andMers863223660
23andMe allrs863223660
SNP Nexus

SNPshotrs863223660
SNPdbers863223660
MSV3drs863223660
GWAS Ctlgrs863223660
Max Magnitude0
ClinVar
Risk rs863223660(G;G)
Alt rs863223660(G;G)
Reference rs863223660(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10620605T>C
CLNSRC
CLNACC RCV000198129.1,