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rs794727953

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727953(C;T)
Make rs794727953(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10650274
GeneJAG1, MIR6870
is asnp
is mentioned by
dbSNPrs794727953
ebirs794727953
HLIrs794727953
Exacrs794727953
Varsomers794727953
Maprs794727953
PheGenIrs794727953
hapmaprs794727953
1000 genomesrs794727953
hgdprs794727953
ensemblrs794727953
gopubmedrs794727953
geneviewrs794727953
scholarrs794727953
googlers794727953
pharmgkbrs794727953
gwascentralrs794727953
openSNPrs794727953
23andMers794727953
23andMe allrs794727953
SNP Nexus

SNPshotrs794727953
SNPdbers794727953
MSV3drs794727953
GWAS Ctlgrs794727953
Max Magnitude0
ClinVar
Risk rs794727953(T;T)
Alt rs794727953(T;T)
Reference rs794727953(C;C)
Significance Pathogenic
Disease Alagille syndrome 1
Variation info
Gene MIR6870 JAG1
CLNDBN Alagille syndrome 1
Reversed 1
HGVS NC_000020.10:g.10630922G>A
CLNSRC
CLNACC RCV000180477.1,