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rs267606762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606762(C;T)
Make rs267606762(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position97598852
GeneHOGA1
is asnp
is mentioned by
dbSNPrs267606762
ebirs267606762
HLIrs267606762
Exacrs267606762
Varsomers267606762
Maprs267606762
PheGenIrs267606762
hapmaprs267606762
1000 genomesrs267606762
hgdprs267606762
ensemblrs267606762
gopubmedrs267606762
geneviewrs267606762
scholarrs267606762
googlers267606762
pharmgkbrs267606762
gwascentralrs267606762
openSNPrs267606762
23andMers267606762
23andMe allrs267606762
SNP Nexus

SNPshotrs267606762
SNPdbers267606762
MSV3drs267606762
GWAS Ctlgrs267606762
Max Magnitude0
ClinVar
Risk rs267606762(T;T)
Alt rs267606762(T;T)
Reference rs267606762(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99358609C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000048.2,