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rs796052087

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052087(C;C)
Make rs796052087(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97611550
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052087
ebirs796052087
HLIrs796052087
Exacrs796052087
Varsomers796052087
Maprs796052087
PheGenIrs796052087
hapmaprs796052087
1000 genomesrs796052087
hgdprs796052087
ensemblrs796052087
gopubmedrs796052087
geneviewrs796052087
scholarrs796052087
googlers796052087
pharmgkbrs796052087
gwascentralrs796052087
openSNPrs796052087
23andMers796052087
23andMe allrs796052087
SNP Nexus

SNPshotrs796052087
SNPdbers796052087
MSV3drs796052087
GWAS Ctlgrs796052087
Max Magnitude0
ClinVar
Risk rs796052087(C;C)
Alt rs796052087(C;C)
Reference rs796052087(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99371307T>C
CLNSRC
CLNACC RCV000186485.1,