Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223672

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223672(-;T)
Make rs863223672(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10644949
GeneJAG1
is asnp
is mentioned by
dbSNPrs863223672
ClinGenrs863223672
ebirs863223672
HLIrs863223672
Exacrs863223672
Varsomers863223672
Maprs863223672
PheGenIrs863223672
hapmaprs863223672
1000 genomesrs863223672
hgdprs863223672
ensemblrs863223672
gopubmedrs863223672
geneviewrs863223672
scholarrs863223672
googlers863223672
pharmgkbrs863223672
gwascentralrs863223672
openSNPrs863223672
23andMers863223672
23andMe allrs863223672
SNP Nexus

SNPshotrs863223672
SNPdbers863223672
MSV3drs863223672
GWAS Ctlgrs863223672
Max Magnitude0
ClinVar
Risk rs863223672(T;T)
Alt rs863223672(T;T)
Reference Rs863223672(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10625598dupA
CLNSRC
CLNACC RCV000200278.1,