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rs756489804

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756489804(C;G)
Make rs756489804(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97611514
GeneHOGA1
is asnp
is mentioned by
dbSNPrs756489804
ebirs756489804
HLIrs756489804
Exacrs756489804
Varsomers756489804
Maprs756489804
PheGenIrs756489804
hapmaprs756489804
1000 genomesrs756489804
hgdprs756489804
ensemblrs756489804
gopubmedrs756489804
geneviewrs756489804
scholarrs756489804
googlers756489804
pharmgkbrs756489804
gwascentralrs756489804
openSNPrs756489804
23andMers756489804
23andMe allrs756489804
SNP Nexus

SNPshotrs756489804
SNPdbers756489804
MSV3drs756489804
GWAS Ctlgrs756489804
Max Magnitude0
ClinVar
Risk rs756489804(G;G)
Alt rs756489804(G;G)
Reference rs756489804(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99371271C>T
CLNSRC
CLNACC RCV000186484.1,