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rs796052079

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052079(A;A)
Make rs796052079(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position37432016
GeneGRHPR
is asnp
is mentioned by
dbSNPrs796052079
ebirs796052079
HLIrs796052079
Exacrs796052079
Varsomers796052079
Maprs796052079
PheGenIrs796052079
hapmaprs796052079
1000 genomesrs796052079
hgdprs796052079
ensemblrs796052079
gopubmedrs796052079
geneviewrs796052079
scholarrs796052079
googlers796052079
pharmgkbrs796052079
gwascentralrs796052079
openSNPrs796052079
23andMers796052079
23andMe allrs796052079
SNP Nexus

SNPshotrs796052079
SNPdbers796052079
MSV3drs796052079
GWAS Ctlgrs796052079
Max Magnitude0
ClinVar
Risk rs796052079(A;A)
Alt rs796052079(A;A)
Reference rs796052079(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37432013T>A
CLNSRC
CLNACC RCV000186443.1,