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rs746155190

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746155190(C;C)
Make rs746155190(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position96189654
GeneSLC25A13
is asnp
is mentioned by
dbSNPrs746155190
ebirs746155190
HLIrs746155190
Exacrs746155190
Varsomers746155190
Maprs746155190
PheGenIrs746155190
hapmaprs746155190
1000 genomesrs746155190
hgdprs746155190
ensemblrs746155190
gopubmedrs746155190
geneviewrs746155190
scholarrs746155190
googlers746155190
pharmgkbrs746155190
gwascentralrs746155190
openSNPrs746155190
23andMers746155190
23andMe allrs746155190
SNP Nexus

SNPshotrs746155190
SNPdbers746155190
MSV3drs746155190
GWAS Ctlgrs746155190
Max Magnitude0
ClinVar
Risk rs746155190(C;C)
Alt rs746155190(C;C)
Reference rs746155190(G;G)
Significance Pathogenic
Disease Neonatal intrahepatic cholestasis caused by citrin deficiency
Variation info
Gene SLC25A13
CLNDBN Neonatal intrahepatic cholestasis caused by citrin deficiency
Reversed 0
HGVS NC_000007.13:g.95818966G>A
CLNSRC
CLNACC RCV000239387.1,