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rs796052092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTG;CTG) 0 common in clinvar
Make rs796052092(-;-)
Make rs796052092(-;TGC)
Make rs796052092(TGC;TGC)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97601959
GeneHOGA1
is asnp
is mentioned by
dbSNPrs796052092
dbSNP (old)rs796052092
ClinGenrs796052092
ebirs796052092
HLIrs796052092
Exacrs796052092
Gnomadrs796052092
Varsomers796052092
Maprs796052092
PheGenIrs796052092
Biobankrs796052092
1000 genomesrs796052092
hgdprs796052092
ensemblrs796052092
gopubmedrs796052092
geneviewrs796052092
scholarrs796052092
googlers796052092
pharmgkbrs796052092
gwascentralrs796052092
openSNPrs796052092
23andMers796052092
23andMe allrs796052092
SNP Nexus

SNPshotrs796052092
SNPdbers796052092
MSV3drs796052092
GWAS Ctlgrs796052092
Max Magnitude0
ClinVar
Risk rs796052092(-;-)
Alt rs796052092(-;-)
Reference Rs796052092(CTG;CTG)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99361716_99361718delTGC
CLNSRC
CLNACC RCV000186495.1,