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rs746419489

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746419489(A;A)
Make rs746419489(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97584820
GeneHOGA1
is asnp
is mentioned by
dbSNPrs746419489
ebirs746419489
HLIrs746419489
Exacrs746419489
Varsomers746419489
Maprs746419489
PheGenIrs746419489
hapmaprs746419489
1000 genomesrs746419489
hgdprs746419489
ensemblrs746419489
gopubmedrs746419489
geneviewrs746419489
scholarrs746419489
googlers746419489
pharmgkbrs746419489
gwascentralrs746419489
openSNPrs746419489
23andMers746419489
23andMe allrs746419489
SNP Nexus

SNPshotrs746419489
SNPdbers746419489
MSV3drs746419489
GWAS Ctlgrs746419489
Max Magnitude0
ClinVar
Risk rs746419489(A;A)
Alt rs746419489(A;A)
Reference rs746419489(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99344577C>A
CLNSRC
CLNACC RCV000186475.1,