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rs796052080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs796052080(-;-)
Make rs796052080(-;CC)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position37424832
GeneGRHPR
is asnp
is mentioned by
dbSNPrs796052080
ClinGenrs796052080
ebirs796052080
HLIrs796052080
Exacrs796052080
Varsomers796052080
Maprs796052080
PheGenIrs796052080
hapmaprs796052080
1000 genomesrs796052080
hgdprs796052080
ensemblrs796052080
gopubmedrs796052080
geneviewrs796052080
scholarrs796052080
googlers796052080
pharmgkbrs796052080
gwascentralrs796052080
openSNPrs796052080
23andMers796052080
23andMe allrs796052080
SNP Nexus

SNPshotrs796052080
SNPdbers796052080
MSV3drs796052080
GWAS Ctlgrs796052080
Max Magnitude0
ClinVar
Risk rs796052080(-;-)
Alt rs796052080(-;-)
Reference Rs796052080(CC;CC)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37424829_37424830delCC
CLNSRC
CLNACC RCV000186453.1,