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rs796052084

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052084(G;G)
Make rs796052084(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97598784
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052084
ebirs796052084
HLIrs796052084
Exacrs796052084
Varsomers796052084
Maprs796052084
PheGenIrs796052084
hapmaprs796052084
1000 genomesrs796052084
hgdprs796052084
ensemblrs796052084
gopubmedrs796052084
geneviewrs796052084
scholarrs796052084
googlers796052084
pharmgkbrs796052084
gwascentralrs796052084
openSNPrs796052084
23andMers796052084
23andMe allrs796052084
SNP Nexus

SNPshotrs796052084
SNPdbers796052084
MSV3drs796052084
GWAS Ctlgrs796052084
Max Magnitude0
ClinVar
Risk rs796052084(G;G)
Alt rs796052084(G;G)
Reference rs796052084(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99358541T>G
CLNSRC
CLNACC RCV000186474.1,