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rs267606764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606764(G;G)
Make rs267606764(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position97601925
GeneHOGA1
is asnp
is mentioned by
dbSNPrs267606764
ebirs267606764
HLIrs267606764
Exacrs267606764
Varsomers267606764
Maprs267606764
PheGenIrs267606764
hapmaprs267606764
1000 genomesrs267606764
hgdprs267606764
ensemblrs267606764
gopubmedrs267606764
geneviewrs267606764
scholarrs267606764
googlers267606764
pharmgkbrs267606764
gwascentralrs267606764
openSNPrs267606764
23andMers267606764
23andMe allrs267606764
SNP Nexus

SNPshotrs267606764
SNPdbers267606764
MSV3drs267606764
GWAS Ctlgrs267606764
Max Magnitude0
ClinVar
Risk rs267606764(G;G)
Alt rs267606764(G;G)
Reference rs267606764(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99361682T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000051.2,