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rs796052058

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052058(A;A)
Make rs796052058(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240869213
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs796052058
ebirs796052058
HLIrs796052058
Exacrs796052058
Varsomers796052058
Maprs796052058
PheGenIrs796052058
hapmaprs796052058
1000 genomesrs796052058
hgdprs796052058
ensemblrs796052058
gopubmedrs796052058
geneviewrs796052058
scholarrs796052058
googlers796052058
pharmgkbrs796052058
gwascentralrs796052058
openSNPrs796052058
23andMers796052058
23andMe allrs796052058
SNP Nexus

SNPshotrs796052058
SNPdbers796052058
MSV3drs796052058
GWAS Ctlgrs796052058
Max Magnitude0
ClinVar
Risk rs796052058(A;A)
Alt rs796052058(A;A)
Reference rs796052058(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808630C>A
CLNSRC
CLNACC RCV000186287.1,