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rs796052057

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052057(C;C)
Make rs796052057(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240868887
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs796052057
ebirs796052057
HLIrs796052057
Exacrs796052057
Varsomers796052057
Maprs796052057
PheGenIrs796052057
hapmaprs796052057
1000 genomesrs796052057
hgdprs796052057
ensemblrs796052057
gopubmedrs796052057
geneviewrs796052057
scholarrs796052057
googlers796052057
pharmgkbrs796052057
gwascentralrs796052057
openSNPrs796052057
23andMers796052057
23andMe allrs796052057
SNP Nexus

SNPshotrs796052057
SNPdbers796052057
MSV3drs796052057
GWAS Ctlgrs796052057
Max Magnitude0
ClinVar
Risk rs796052057(C;C)
Alt rs796052057(C;C)
Reference rs796052057(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808304G>C
CLNSRC
CLNACC RCV000186273.1,