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rs796052086

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052086(C;T)
Make rs796052086(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97601919
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052086
ebirs796052086
HLIrs796052086
Exacrs796052086
Varsomers796052086
Maprs796052086
PheGenIrs796052086
hapmaprs796052086
1000 genomesrs796052086
hgdprs796052086
ensemblrs796052086
gopubmedrs796052086
geneviewrs796052086
scholarrs796052086
googlers796052086
pharmgkbrs796052086
gwascentralrs796052086
openSNPrs796052086
23andMers796052086
23andMe allrs796052086
SNP Nexus

SNPshotrs796052086
SNPdbers796052086
MSV3drs796052086
GWAS Ctlgrs796052086
Max Magnitude0
ClinVar
Risk rs796052086(T;T)
Alt rs796052086(T;T)
Reference rs796052086(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99361676C>T
CLNSRC
CLNACC RCV000186483.1,