Have questions? Visit https://www.reddit.com/r/SNPedia

rs876660979

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660979(A;A)
Make rs876660979(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10658467
GeneJAG1
is asnp
is mentioned by
dbSNPrs876660979
ebirs876660979
HLIrs876660979
Exacrs876660979
Varsomers876660979
Maprs876660979
PheGenIrs876660979
hapmaprs876660979
1000 genomesrs876660979
hgdprs876660979
ensemblrs876660979
gopubmedrs876660979
geneviewrs876660979
scholarrs876660979
googlers876660979
pharmgkbrs876660979
gwascentralrs876660979
openSNPrs876660979
23andMers876660979
23andMe allrs876660979
SNP Nexus

SNPshotrs876660979
SNPdbers876660979
MSV3drs876660979
GWAS Ctlgrs876660979
Max Magnitude0
ClinVar
Risk rs876660979(A;A)
Alt rs876660979(A;A)
Reference rs876660979(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10639115C>T
CLNSRC
CLNACC RCV000216385.1,