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rs863223647

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223647(A;A)
Make rs863223647(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10673528
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223647
ebirs863223647
HLIrs863223647
Exacrs863223647
Varsomers863223647
Maprs863223647
PheGenIrs863223647
hapmaprs863223647
1000 genomesrs863223647
hgdprs863223647
ensemblrs863223647
gopubmedrs863223647
geneviewrs863223647
scholarrs863223647
googlers863223647
pharmgkbrs863223647
gwascentralrs863223647
openSNPrs863223647
23andMers863223647
23andMe allrs863223647
SNP Nexus

SNPshotrs863223647
SNPdbers863223647
MSV3drs863223647
GWAS Ctlgrs863223647
Max Magnitude0
ClinVar
Risk rs863223647(A;A)
Alt rs863223647(A;A)
Reference rs863223647(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10654176C>T
CLNSRC
CLNACC RCV000197790.1,