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rs267606763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606763(C;C)
Make rs267606763(C;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position97584912
GeneHOGA1
is asnp
is mentioned by
dbSNPrs267606763
ebirs267606763
HLIrs267606763
Exacrs267606763
Varsomers267606763
Maprs267606763
PheGenIrs267606763
hapmaprs267606763
1000 genomesrs267606763
hgdprs267606763
ensemblrs267606763
gopubmedrs267606763
geneviewrs267606763
scholarrs267606763
googlers267606763
pharmgkbrs267606763
gwascentralrs267606763
openSNPrs267606763
23andMers267606763
23andMe allrs267606763
SNP Nexus

SNPshotrs267606763
SNPdbers267606763
MSV3drs267606763
GWAS Ctlgrs267606763
Max Magnitude0
ClinVar
Risk rs267606763(C;C)
Alt rs267606763(C;C)
Reference rs267606763(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99344669G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000050.2,