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rs876661121

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661121(G;T)
Make rs876661121(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641112
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661121
ebirs876661121
HLIrs876661121
Exacrs876661121
Varsomers876661121
Maprs876661121
PheGenIrs876661121
hapmaprs876661121
1000 genomesrs876661121
hgdprs876661121
ensemblrs876661121
gopubmedrs876661121
geneviewrs876661121
scholarrs876661121
googlers876661121
pharmgkbrs876661121
gwascentralrs876661121
openSNPrs876661121
23andMers876661121
23andMe allrs876661121
SNP Nexus

SNPshotrs876661121
SNPdbers876661121
MSV3drs876661121
GWAS Ctlgrs876661121
Max Magnitude0
ClinVar
Risk rs876661121(T;T)
Alt rs876661121(T;T)
Reference rs876661121(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10621760C>A
CLNSRC
CLNACC RCV000219290.1,