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rs796052091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052091(-;-)
Make rs796052091(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97584861
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052091
dbSNP (classic)rs796052091
ClinGenrs796052091
ebirs796052091
HLIrs796052091
Exacrs796052091
Gnomadrs796052091
Varsomers796052091
LitVarrs796052091
Maprs796052091
PheGenIrs796052091
Biobankrs796052091
1000 genomesrs796052091
hgdprs796052091
ensemblrs796052091
geneviewrs796052091
scholarrs796052091
googlers796052091
pharmgkbrs796052091
gwascentralrs796052091
openSNPrs796052091
23andMers796052091
SNPshotrs796052091
SNPdbers796052091
MSV3drs796052091
GWAS Ctlgrs796052091
Max Magnitude0
ClinVar
Risk rs796052091(-;-)
Alt rs796052091(-;-)
Reference Rs796052091(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99344618delA
CLNSRC
CLNACC RCV000186494.1,