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rs796052062

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052062(A;A)
Make rs796052062(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240873049
GeneAGXT
is asnp
is mentioned by
dbSNPrs796052062
ebirs796052062
HLIrs796052062
Exacrs796052062
Varsomers796052062
Maprs796052062
PheGenIrs796052062
hapmaprs796052062
1000 genomesrs796052062
hgdprs796052062
ensemblrs796052062
gopubmedrs796052062
geneviewrs796052062
scholarrs796052062
googlers796052062
pharmgkbrs796052062
gwascentralrs796052062
openSNPrs796052062
23andMers796052062
23andMe allrs796052062
SNP Nexus

SNPshotrs796052062
SNPdbers796052062
MSV3drs796052062
GWAS Ctlgrs796052062
Max Magnitude0
ClinVar
Risk rs796052062(A;A)
Alt rs796052062(A;A)
Reference rs796052062(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812466G>A
CLNSRC
CLNACC RCV000186320.1,