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rs863223666

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223666(-;C)
Make rs863223666(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10672895
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223666
ClinGenrs863223666
ebirs863223666
HLIrs863223666
Exacrs863223666
Varsomers863223666
Maprs863223666
PheGenIrs863223666
hapmaprs863223666
1000 genomesrs863223666
hgdprs863223666
ensemblrs863223666
gopubmedrs863223666
geneviewrs863223666
scholarrs863223666
googlers863223666
pharmgkbrs863223666
gwascentralrs863223666
openSNPrs863223666
23andMers863223666
23andMe allrs863223666
SNP Nexus

SNPshotrs863223666
SNPdbers863223666
MSV3drs863223666
GWAS Ctlgrs863223666
Max Magnitude0
ClinVar
Risk rs863223666(C;C)
Alt rs863223666(C;C)
Reference Rs863223666(;)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10653544dupG
CLNSRC
CLNACC RCV000196170.1,