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rs863223649

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223649(C;T)
Make rs863223649(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10652227
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223649
ebirs863223649
HLIrs863223649
Exacrs863223649
Varsomers863223649
Maprs863223649
PheGenIrs863223649
hapmaprs863223649
1000 genomesrs863223649
hgdprs863223649
ensemblrs863223649
gopubmedrs863223649
geneviewrs863223649
scholarrs863223649
googlers863223649
pharmgkbrs863223649
gwascentralrs863223649
openSNPrs863223649
23andMers863223649
23andMe allrs863223649
SNP Nexus

SNPshotrs863223649
SNPdbers863223649
MSV3drs863223649
GWAS Ctlgrs863223649
Max Magnitude0
ClinVar
Risk rs863223649(T;T)
Alt rs863223649(T;T)
Reference rs863223649(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10632875G>A
CLNSRC
CLNACC RCV000198219.1,