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rs876661229

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661229(A;A)
Make rs876661229(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10645424
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661229
ebirs876661229
HLIrs876661229
Exacrs876661229
Varsomers876661229
Maprs876661229
PheGenIrs876661229
hapmaprs876661229
1000 genomesrs876661229
hgdprs876661229
ensemblrs876661229
gopubmedrs876661229
geneviewrs876661229
scholarrs876661229
googlers876661229
pharmgkbrs876661229
gwascentralrs876661229
openSNPrs876661229
23andMers876661229
23andMe allrs876661229
SNP Nexus

SNPshotrs876661229
SNPdbers876661229
MSV3drs876661229
GWAS Ctlgrs876661229
Max Magnitude0
ClinVar
Risk rs876661229(A;A)
Alt rs876661229(A;A)
Reference rs876661229(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10626072C>T
CLNSRC
CLNACC RCV000223007.1,