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rs876661165

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661165(-;-)
Make rs876661165(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10643818
GeneJAG1
is asnp
is mentioned by
dbSNPrs876661165
ebirs876661165
HLIrs876661165
Exacrs876661165
Varsomers876661165
Maprs876661165
PheGenIrs876661165
hapmaprs876661165
1000 genomesrs876661165
hgdprs876661165
ensemblrs876661165
gopubmedrs876661165
geneviewrs876661165
scholarrs876661165
googlers876661165
pharmgkbrs876661165
gwascentralrs876661165
openSNPrs876661165
23andMers876661165
23andMe allrs876661165
SNP Nexus

SNPshotrs876661165
SNPdbers876661165
MSV3drs876661165
GWAS Ctlgrs876661165
Max Magnitude0
ClinVar
Risk rs876661165(;)
Alt rs876661165(;)
Reference rs876661165(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene JAG1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.10624466delG
CLNSRC
CLNACC RCV000215073.1,