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rs796052074

From SNPedia

Orientationplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs796052074(-;-)
Make rs796052074(-;CA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240878038
GeneAGXT
is asnp
is mentioned by
dbSNPrs796052074
ebirs796052074
HLIrs796052074
Exacrs796052074
Varsomers796052074
Maprs796052074
PheGenIrs796052074
hapmaprs796052074
1000 genomesrs796052074
hgdprs796052074
ensemblrs796052074
gopubmedrs796052074
geneviewrs796052074
scholarrs796052074
googlers796052074
pharmgkbrs796052074
gwascentralrs796052074
openSNPrs796052074
23andMers796052074
23andMe allrs796052074
SNP Nexus

SNPshotrs796052074
SNPdbers796052074
MSV3drs796052074
GWAS Ctlgrs796052074
Max Magnitude0
ClinVar
Risk rs796052074(;)
Alt rs796052074(;)
Reference rs796052074(CA;CA)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817455_241817456delCA
CLNSRC
CLNACC RCV000186415.1,