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rs755562733

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755562733(G;T)
Make rs755562733(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97601889
GeneHOGA1
is asnp
is mentioned by
dbSNPrs755562733
ebirs755562733
HLIrs755562733
Exacrs755562733
Varsomers755562733
Maprs755562733
PheGenIrs755562733
hapmaprs755562733
1000 genomesrs755562733
hgdprs755562733
ensemblrs755562733
gopubmedrs755562733
geneviewrs755562733
scholarrs755562733
googlers755562733
pharmgkbrs755562733
gwascentralrs755562733
openSNPrs755562733
23andMers755562733
23andMe allrs755562733
SNP Nexus

SNPshotrs755562733
SNPdbers755562733
MSV3drs755562733
GWAS Ctlgrs755562733
Max Magnitude0
ClinVar
Risk rs755562733(A,T;A,T)
Alt rs755562733(A,T;A,T)
Reference rs755562733(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99361646G>A
CLNSRC
CLNACC RCV000186482.1,