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rs796052066

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052066(A;A)
Make rs796052066(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240878790
GeneAGXT
is asnp
is mentioned by
dbSNPrs796052066
ebirs796052066
HLIrs796052066
Exacrs796052066
Varsomers796052066
Maprs796052066
PheGenIrs796052066
hapmaprs796052066
1000 genomesrs796052066
hgdprs796052066
ensemblrs796052066
gopubmedrs796052066
geneviewrs796052066
scholarrs796052066
googlers796052066
pharmgkbrs796052066
gwascentralrs796052066
openSNPrs796052066
23andMers796052066
23andMe allrs796052066
SNP Nexus

SNPshotrs796052066
SNPdbers796052066
MSV3drs796052066
GWAS Ctlgrs796052066
Max Magnitude0
ClinVar
Risk rs796052066(A;A)
Alt rs796052066(A;A)
Reference rs796052066(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241818207C>A
CLNSRC
CLNACC RCV000186356.1,