Have questions? Visit https://www.reddit.com/r/SNPedia

rs764396564

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764396564(C;T)
Make rs764396564(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97584837
GeneHOGA1
is asnp
is mentioned by
dbSNPrs764396564
ebirs764396564
HLIrs764396564
Exacrs764396564
Varsomers764396564
Maprs764396564
PheGenIrs764396564
hapmaprs764396564
1000 genomesrs764396564
hgdprs764396564
ensemblrs764396564
gopubmedrs764396564
geneviewrs764396564
scholarrs764396564
googlers764396564
pharmgkbrs764396564
gwascentralrs764396564
openSNPrs764396564
23andMers764396564
23andMe allrs764396564
SNP Nexus

SNPshotrs764396564
SNPdbers764396564
MSV3drs764396564
GWAS Ctlgrs764396564
Max Magnitude0
ClinVar
Risk rs764396564(T;T)
Alt rs764396564(T;T)
Reference rs764396564(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99344594C>T
CLNSRC
CLNACC RCV000186473.1,