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rs876661182

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661182(A;T)
Make rs876661182(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641193
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661182
ebirs876661182
HLIrs876661182
Exacrs876661182
Varsomers876661182
Maprs876661182
PheGenIrs876661182
hapmaprs876661182
1000 genomesrs876661182
hgdprs876661182
ensemblrs876661182
gopubmedrs876661182
geneviewrs876661182
scholarrs876661182
googlers876661182
pharmgkbrs876661182
gwascentralrs876661182
openSNPrs876661182
23andMers876661182
23andMe allrs876661182
SNP Nexus

SNPshotrs876661182
SNPdbers876661182
MSV3drs876661182
GWAS Ctlgrs876661182
Max Magnitude0
ClinVar
Risk rs876661182(T;T)
Alt rs876661182(T;T)
Reference rs876661182(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10621841T>A
CLNSRC
CLNACC RCV000221278.1,