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rs796052065

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052065(A;A)
Make rs796052065(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240878124
GeneAGXT
is asnp
is mentioned by
dbSNPrs796052065
ebirs796052065
HLIrs796052065
Exacrs796052065
Varsomers796052065
Maprs796052065
PheGenIrs796052065
hapmaprs796052065
1000 genomesrs796052065
hgdprs796052065
ensemblrs796052065
gopubmedrs796052065
geneviewrs796052065
scholarrs796052065
googlers796052065
pharmgkbrs796052065
gwascentralrs796052065
openSNPrs796052065
23andMers796052065
23andMe allrs796052065
SNP Nexus

SNPshotrs796052065
SNPdbers796052065
MSV3drs796052065
GWAS Ctlgrs796052065
Max Magnitude0
ClinVar
Risk rs796052065(A;A)
Alt rs796052065(A;A)
Reference rs796052065(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817541G>A
CLNSRC
CLNACC RCV000186352.1,