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rs878853752

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853752(-;-)
Make rs878853752(-;T)
Make rs878853752(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10641480
GeneJAG1
is asnp
is mentioned by
dbSNPrs878853752
ebirs878853752
HLIrs878853752
Exacrs878853752
Varsomers878853752
Maprs878853752
PheGenIrs878853752
hapmaprs878853752
1000 genomesrs878853752
hgdprs878853752
ensemblrs878853752
gopubmedrs878853752
geneviewrs878853752
scholarrs878853752
googlers878853752
pharmgkbrs878853752
gwascentralrs878853752
openSNPrs878853752
23andMers878853752
23andMe allrs878853752
SNP Nexus

SNPshotrs878853752
SNPdbers878853752
MSV3drs878853752
GWAS Ctlgrs878853752
Max Magnitude0
ClinVar
Risk rs878853752(T;T)
Alt rs878853752(T;T)
Reference rs878853752(;)
Significance Pathogenic
Disease Alagille syndrome 1
Variation info
Gene JAG1
CLNDBN Alagille syndrome 1
Reversed 1
HGVS NC_000020.10:g.10622129dupA
CLNSRC
CLNACC RCV000233877.1,