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rs796052089

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052089(A;T)
Make rs796052089(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97598871
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052089
ebirs796052089
HLIrs796052089
Exacrs796052089
Varsomers796052089
Maprs796052089
PheGenIrs796052089
hapmaprs796052089
1000 genomesrs796052089
hgdprs796052089
ensemblrs796052089
gopubmedrs796052089
geneviewrs796052089
scholarrs796052089
googlers796052089
pharmgkbrs796052089
gwascentralrs796052089
openSNPrs796052089
23andMers796052089
23andMe allrs796052089
SNP Nexus

SNPshotrs796052089
SNPdbers796052089
MSV3drs796052089
GWAS Ctlgrs796052089
Max Magnitude0
ClinVar
Risk rs796052089(T;T)
Alt rs796052089(T;T)
Reference rs796052089(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99358628A>T
CLNSRC
CLNACC RCV000186488.1,