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rs796052085

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052085(A;A)
Make rs796052085(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97601884
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052085
ebirs796052085
HLIrs796052085
Exacrs796052085
Varsomers796052085
Maprs796052085
PheGenIrs796052085
hapmaprs796052085
1000 genomesrs796052085
hgdprs796052085
ensemblrs796052085
gopubmedrs796052085
geneviewrs796052085
scholarrs796052085
googlers796052085
pharmgkbrs796052085
gwascentralrs796052085
openSNPrs796052085
23andMers796052085
23andMe allrs796052085
SNP Nexus

SNPshotrs796052085
SNPdbers796052085
MSV3drs796052085
GWAS Ctlgrs796052085
Max Magnitude0
ClinVar
Risk rs796052085(A;A)
Alt rs796052085(A;A)
Reference rs796052085(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99361641C>A
CLNSRC
CLNACC RCV000186481.1,