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rs777046879

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777046879(A;A)
Make rs777046879(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97611648
GeneHOGA1
is asnp
is mentioned by
dbSNPrs777046879
ebirs777046879
HLIrs777046879
Exacrs777046879
Varsomers777046879
Maprs777046879
PheGenIrs777046879
hapmaprs777046879
1000 genomesrs777046879
hgdprs777046879
ensemblrs777046879
gopubmedrs777046879
geneviewrs777046879
scholarrs777046879
googlers777046879
pharmgkbrs777046879
gwascentralrs777046879
openSNPrs777046879
23andMers777046879
23andMe allrs777046879
SNP Nexus

SNPshotrs777046879
SNPdbers777046879
MSV3drs777046879
GWAS Ctlgrs777046879
Max Magnitude0
ClinVar
Risk rs777046879(A;A)
Alt rs777046879(A;A)
Reference rs777046879(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99371405G>A
CLNSRC
CLNACC RCV000186491.1,