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rs863223651

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223651(C;C)
Make rs863223651(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10649531
GeneJAG1, MIR6870
is asnp
is mentioned by
dbSNPrs863223651
ebirs863223651
HLIrs863223651
Exacrs863223651
Varsomers863223651
Maprs863223651
PheGenIrs863223651
hapmaprs863223651
1000 genomesrs863223651
hgdprs863223651
ensemblrs863223651
gopubmedrs863223651
geneviewrs863223651
scholarrs863223651
googlers863223651
pharmgkbrs863223651
gwascentralrs863223651
openSNPrs863223651
23andMers863223651
23andMe allrs863223651
SNP Nexus

SNPshotrs863223651
SNPdbers863223651
MSV3drs863223651
GWAS Ctlgrs863223651
Max Magnitude0
ClinVar
Risk rs863223651(C;C)
Alt rs863223651(C;C)
Reference rs863223651(T;T)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MIR6870 JAG1
CLNDBN not provided not specified
Reversed 1
HGVS NC_000020.10:g.10630179A>G
CLNSRC
CLNACC RCV000196545.1, RCV000223845.1,