Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052068

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052068(A;G)
Make rs796052068(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240875933
GeneAGXT
is asnp
is mentioned by
dbSNPrs796052068
ebirs796052068
HLIrs796052068
Exacrs796052068
Varsomers796052068
Maprs796052068
PheGenIrs796052068
hapmaprs796052068
1000 genomesrs796052068
hgdprs796052068
ensemblrs796052068
gopubmedrs796052068
geneviewrs796052068
scholarrs796052068
googlers796052068
pharmgkbrs796052068
gwascentralrs796052068
openSNPrs796052068
23andMers796052068
23andMe allrs796052068
SNP Nexus

SNPshotrs796052068
SNPdbers796052068
MSV3drs796052068
GWAS Ctlgrs796052068
Max Magnitude0
ClinVar
Risk rs796052068(G;G)
Alt rs796052068(G;G)
Reference rs796052068(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815350A>G
CLNSRC
CLNACC RCV000186374.1,