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rs796052059

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052059(A;A)
Make rs796052059(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240869258
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs796052059
ebirs796052059
HLIrs796052059
Exacrs796052059
Varsomers796052059
Maprs796052059
PheGenIrs796052059
hapmaprs796052059
1000 genomesrs796052059
hgdprs796052059
ensemblrs796052059
gopubmedrs796052059
geneviewrs796052059
scholarrs796052059
googlers796052059
pharmgkbrs796052059
gwascentralrs796052059
openSNPrs796052059
23andMers796052059
23andMe allrs796052059
SNP Nexus

SNPshotrs796052059
SNPdbers796052059
MSV3drs796052059
GWAS Ctlgrs796052059
Max Magnitude0
ClinVar
Risk rs796052059(A;A)
Alt rs796052059(A;A)
Reference rs796052059(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808675C>A
CLNSRC
CLNACC RCV000186292.1,