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rs796052073

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052073(A;A)
Make rs796052073(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240875988
GeneAGXT
is asnp
is mentioned by
dbSNPrs796052073
ebirs796052073
HLIrs796052073
Exacrs796052073
Varsomers796052073
Maprs796052073
PheGenIrs796052073
hapmaprs796052073
1000 genomesrs796052073
hgdprs796052073
ensemblrs796052073
gopubmedrs796052073
geneviewrs796052073
scholarrs796052073
googlers796052073
pharmgkbrs796052073
gwascentralrs796052073
openSNPrs796052073
23andMers796052073
23andMe allrs796052073
SNP Nexus

SNPshotrs796052073
SNPdbers796052073
MSV3drs796052073
GWAS Ctlgrs796052073
Max Magnitude0
ClinVar
Risk rs796052073(A;A)
Alt rs796052073(A;A)
Reference rs796052073(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815405C>A
CLNSRC
CLNACC RCV000186409.1,