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rs876661096

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661096(C;T)
Make rs876661096(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10652483
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661096
ebirs876661096
HLIrs876661096
Exacrs876661096
Varsomers876661096
Maprs876661096
PheGenIrs876661096
hapmaprs876661096
1000 genomesrs876661096
hgdprs876661096
ensemblrs876661096
gopubmedrs876661096
geneviewrs876661096
scholarrs876661096
googlers876661096
pharmgkbrs876661096
gwascentralrs876661096
openSNPrs876661096
23andMers876661096
23andMe allrs876661096
SNP Nexus

SNPshotrs876661096
SNPdbers876661096
MSV3drs876661096
GWAS Ctlgrs876661096
Max Magnitude0
ClinVar
Risk rs876661096(T;T)
Alt rs876661096(T;T)
Reference rs876661096(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10633131G>A
CLNSRC
CLNACC RCV000220558.1,