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rs796052078

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052078(G;T)
Make rs796052078(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position37425994
GeneGRHPR
is asnp
is mentioned by
dbSNPrs796052078
ebirs796052078
HLIrs796052078
Exacrs796052078
Varsomers796052078
Maprs796052078
PheGenIrs796052078
hapmaprs796052078
1000 genomesrs796052078
hgdprs796052078
ensemblrs796052078
gopubmedrs796052078
geneviewrs796052078
scholarrs796052078
googlers796052078
pharmgkbrs796052078
gwascentralrs796052078
openSNPrs796052078
23andMers796052078
23andMe allrs796052078
SNP Nexus

SNPshotrs796052078
SNPdbers796052078
MSV3drs796052078
GWAS Ctlgrs796052078
Max Magnitude0
ClinVar
Risk rs796052078(T;T)
Alt rs796052078(T;T)
Reference rs796052078(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene GRHPR
CLNDBN Primary hyperoxaluria, type II
Reversed 0
HGVS NC_000009.11:g.37425991G>T
CLNSRC
CLNACC RCV000186440.1,