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rs876661061

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661061(C;T)
Make rs876661061(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10642494
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661061
ebirs876661061
HLIrs876661061
Exacrs876661061
Varsomers876661061
Maprs876661061
PheGenIrs876661061
hapmaprs876661061
1000 genomesrs876661061
hgdprs876661061
ensemblrs876661061
gopubmedrs876661061
geneviewrs876661061
scholarrs876661061
googlers876661061
pharmgkbrs876661061
gwascentralrs876661061
openSNPrs876661061
23andMers876661061
23andMe allrs876661061
SNP Nexus

SNPshotrs876661061
SNPdbers876661061
MSV3drs876661061
GWAS Ctlgrs876661061
Max Magnitude0
ClinVar
Risk rs876661061(T;T)
Alt rs876661061(T;T)
Reference rs876661061(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10623142G>A
CLNSRC
CLNACC RCV000218214.1,