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rs876661066

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661066(A;A)
Make rs876661066(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10673449
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661066
ebirs876661066
HLIrs876661066
Exacrs876661066
Varsomers876661066
Maprs876661066
PheGenIrs876661066
hapmaprs876661066
1000 genomesrs876661066
hgdprs876661066
ensemblrs876661066
gopubmedrs876661066
geneviewrs876661066
scholarrs876661066
googlers876661066
pharmgkbrs876661066
gwascentralrs876661066
openSNPrs876661066
23andMers876661066
23andMe allrs876661066
SNP Nexus

SNPshotrs876661066
SNPdbers876661066
MSV3drs876661066
GWAS Ctlgrs876661066
Max Magnitude0
ClinVar
Risk rs876661066(A;A)
Alt rs876661066(A;A)
Reference rs876661066(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10654097C>T
CLNSRC
CLNACC RCV000221204.1,