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rs876660977

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660977(C;C)
Make rs876660977(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10673469
GeneJAG1
is asnp
is mentioned by
dbSNPrs876660977
ebirs876660977
HLIrs876660977
Exacrs876660977
Varsomers876660977
Maprs876660977
PheGenIrs876660977
hapmaprs876660977
1000 genomesrs876660977
hgdprs876660977
ensemblrs876660977
gopubmedrs876660977
geneviewrs876660977
scholarrs876660977
googlers876660977
pharmgkbrs876660977
gwascentralrs876660977
openSNPrs876660977
23andMers876660977
23andMe allrs876660977
SNP Nexus

SNPshotrs876660977
SNPdbers876660977
MSV3drs876660977
GWAS Ctlgrs876660977
Max Magnitude0
ClinVar
Risk rs876660977(C;C)
Alt rs876660977(C;C)
Reference rs876660977(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10654117A>G
CLNSRC
CLNACC RCV000218438.1,