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rs796052088

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052088(A;A)
Make rs796052088(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97598790
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052088
ebirs796052088
HLIrs796052088
Exacrs796052088
Varsomers796052088
Maprs796052088
PheGenIrs796052088
hapmaprs796052088
1000 genomesrs796052088
hgdprs796052088
ensemblrs796052088
gopubmedrs796052088
geneviewrs796052088
scholarrs796052088
googlers796052088
pharmgkbrs796052088
gwascentralrs796052088
openSNPrs796052088
23andMers796052088
23andMe allrs796052088
SNP Nexus

SNPshotrs796052088
SNPdbers796052088
MSV3drs796052088
GWAS Ctlgrs796052088
Max Magnitude0
ClinVar
Risk rs796052088(A;A)
Alt rs796052088(A;A)
Reference rs796052088(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99358547G>A
CLNSRC
CLNACC RCV000186487.1,