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rs796052064

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052064(A;A)
Make rs796052064(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240878075
GeneAGXT
is asnp
is mentioned by
dbSNPrs796052064
ebirs796052064
HLIrs796052064
Exacrs796052064
Varsomers796052064
Maprs796052064
PheGenIrs796052064
hapmaprs796052064
1000 genomesrs796052064
hgdprs796052064
ensemblrs796052064
gopubmedrs796052064
geneviewrs796052064
scholarrs796052064
googlers796052064
pharmgkbrs796052064
gwascentralrs796052064
openSNPrs796052064
23andMers796052064
23andMe allrs796052064
SNP Nexus

SNPshotrs796052064
SNPdbers796052064
MSV3drs796052064
GWAS Ctlgrs796052064
Max Magnitude0
ClinVar
Risk rs796052064(A;A)
Alt rs796052064(A;A)
Reference rs796052064(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817492G>A
CLNSRC
CLNACC RCV000186348.1,