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rs796052090

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052090(C;C)
Make rs796052090(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97599744
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052090
ebirs796052090
HLIrs796052090
Exacrs796052090
Varsomers796052090
Maprs796052090
PheGenIrs796052090
hapmaprs796052090
1000 genomesrs796052090
hgdprs796052090
ensemblrs796052090
gopubmedrs796052090
geneviewrs796052090
scholarrs796052090
googlers796052090
pharmgkbrs796052090
gwascentralrs796052090
openSNPrs796052090
23andMers796052090
23andMe allrs796052090
SNP Nexus

SNPshotrs796052090
SNPdbers796052090
MSV3drs796052090
GWAS Ctlgrs796052090
Max Magnitude0
ClinVar
Risk rs796052090(C;C)
Alt rs796052090(C;C)
Reference rs796052090(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99359501T>C
CLNSRC
CLNACC RCV000186489.1,