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rs863223658

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223658(G;G)
Make rs863223658(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641627
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223658
ebirs863223658
HLIrs863223658
Exacrs863223658
Varsomers863223658
Maprs863223658
PheGenIrs863223658
hapmaprs863223658
1000 genomesrs863223658
hgdprs863223658
ensemblrs863223658
gopubmedrs863223658
geneviewrs863223658
scholarrs863223658
googlers863223658
pharmgkbrs863223658
gwascentralrs863223658
openSNPrs863223658
23andMers863223658
23andMe allrs863223658
SNP Nexus

SNPshotrs863223658
SNPdbers863223658
MSV3drs863223658
GWAS Ctlgrs863223658
Max Magnitude0
ClinVar
Risk rs863223658(G;G)
Alt rs863223658(G;G)
Reference rs863223658(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10622275A>C
CLNSRC
CLNACC RCV000196919.1,