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rs374327791

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374327791(C;T)
Make rs374327791(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97599746
GeneHOGA1
is asnp
is mentioned by
dbSNPrs374327791
ebirs374327791
HLIrs374327791
Exacrs374327791
Varsomers374327791
Maprs374327791
PheGenIrs374327791
hapmaprs374327791
1000 genomesrs374327791
hgdprs374327791
ensemblrs374327791
gopubmedrs374327791
geneviewrs374327791
scholarrs374327791
googlers374327791
pharmgkbrs374327791
gwascentralrs374327791
openSNPrs374327791
23andMers374327791
23andMe allrs374327791
SNP Nexus

SNPshotrs374327791
SNPdbers374327791
MSV3drs374327791
GWAS Ctlgrs374327791
Max Magnitude0
ClinVar
Risk rs374327791(A,T;A,T)
Alt rs374327791(A,T;A,T)
Reference rs374327791(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99359503C>A
CLNSRC
CLNACC RCV000186490.1,