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rs777601935

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777601935(C;C)
Make rs777601935(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97599740
GeneHOGA1
is asnp
is mentioned by
dbSNPrs777601935
ebirs777601935
HLIrs777601935
Exacrs777601935
Varsomers777601935
Maprs777601935
PheGenIrs777601935
hapmaprs777601935
1000 genomesrs777601935
hgdprs777601935
ensemblrs777601935
gopubmedrs777601935
geneviewrs777601935
scholarrs777601935
googlers777601935
pharmgkbrs777601935
gwascentralrs777601935
openSNPrs777601935
23andMers777601935
23andMe allrs777601935
SNP Nexus

SNPshotrs777601935
SNPdbers777601935
MSV3drs777601935
GWAS Ctlgrs777601935
Max Magnitude0
ClinVar
Risk rs777601935(C,T;C,T)
Alt rs777601935(C,T;C,T)
Reference rs777601935(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99359497G>T
CLNSRC
CLNACC RCV000186479.1,