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rs796052081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTA;GTA) 0 common in clinvar
Make rs796052081(-;-)
Make rs796052081(-;AGT)
Make rs796052081(AGT;AGT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position37426536
GeneGRHPR
is asnp
is mentioned by
dbSNPrs796052081
ClinGenrs796052081
ebirs796052081
HLIrs796052081
Exacrs796052081
Varsomers796052081
Maprs796052081
PheGenIrs796052081
hapmaprs796052081
1000 genomesrs796052081
hgdprs796052081
ensemblrs796052081
gopubmedrs796052081
geneviewrs796052081
scholarrs796052081
googlers796052081
pharmgkbrs796052081
gwascentralrs796052081
openSNPrs796052081
23andMers796052081
23andMe allrs796052081
SNP Nexus

SNPshotrs796052081
SNPdbers796052081
MSV3drs796052081
GWAS Ctlgrs796052081
Max Magnitude0
ClinVar
Risk rs796052081(-;-)
Alt rs796052081(-;-)
Reference Rs796052081(GTA;GTA)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37426533_37426535delAGT
CLNSRC
CLNACC RCV000186454.1,