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

rs876661123

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661123(A;A)
Make rs876661123(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10672991
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661123
ebirs876661123
HLIrs876661123
Exacrs876661123
Varsomers876661123
Maprs876661123
PheGenIrs876661123
hapmaprs876661123
1000 genomesrs876661123
hgdprs876661123
ensemblrs876661123
gopubmedrs876661123
geneviewrs876661123
scholarrs876661123
googlers876661123
pharmgkbrs876661123
gwascentralrs876661123
openSNPrs876661123
23andMers876661123
23andMe allrs876661123
SNP Nexus

SNPshotrs876661123
SNPdbers876661123
MSV3drs876661123
GWAS Ctlgrs876661123
Max Magnitude0
ClinVar
Risk rs876661123(A;A)
Alt rs876661123(A;A)
Reference rs876661123(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10653639C>T
CLNSRC
CLNACC RCV000218915.1,