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rs876661142

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661142(A;T)
Make rs876661142(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10645389
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661142
ebirs876661142
HLIrs876661142
Exacrs876661142
Varsomers876661142
Maprs876661142
PheGenIrs876661142
hapmaprs876661142
1000 genomesrs876661142
hgdprs876661142
ensemblrs876661142
gopubmedrs876661142
geneviewrs876661142
scholarrs876661142
googlers876661142
pharmgkbrs876661142
gwascentralrs876661142
openSNPrs876661142
23andMers876661142
23andMe allrs876661142
SNP Nexus

SNPshotrs876661142
SNPdbers876661142
MSV3drs876661142
GWAS Ctlgrs876661142
Max Magnitude0
ClinVar
Risk rs876661142(T;T)
Alt rs876661142(T;T)
Reference rs876661142(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10626037T>A
CLNSRC
CLNACC RCV000221335.1,