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rs876661095

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661095(-;-)
Make rs876661095(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10640920
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661095
ebirs876661095
HLIrs876661095
Exacrs876661095
Varsomers876661095
Maprs876661095
PheGenIrs876661095
hapmaprs876661095
1000 genomesrs876661095
hgdprs876661095
ensemblrs876661095
gopubmedrs876661095
geneviewrs876661095
scholarrs876661095
googlers876661095
pharmgkbrs876661095
gwascentralrs876661095
openSNPrs876661095
23andMers876661095
23andMe allrs876661095
SNP Nexus

SNPshotrs876661095
SNPdbers876661095
MSV3drs876661095
GWAS Ctlgrs876661095
Max Magnitude0
ClinVar
Risk rs876661095(;)
Alt rs876661095(;)
Reference rs876661095(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10621568delA
CLNSRC
CLNACC RCV000216887.1,