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rs796052069

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052069(-;-)
Make rs796052069(-;A)
Make rs796052069(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240869219
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs796052069
ebirs796052069
HLIrs796052069
Exacrs796052069
Varsomers796052069
Maprs796052069
PheGenIrs796052069
hapmaprs796052069
1000 genomesrs796052069
hgdprs796052069
ensemblrs796052069
gopubmedrs796052069
geneviewrs796052069
scholarrs796052069
googlers796052069
pharmgkbrs796052069
gwascentralrs796052069
openSNPrs796052069
23andMers796052069
23andMe allrs796052069
SNP Nexus

SNPshotrs796052069
SNPdbers796052069
MSV3drs796052069
GWAS Ctlgrs796052069
Max Magnitude0
ClinVar
Risk rs796052069(A;A)
Alt rs796052069(A;A)
Reference rs796052069(;)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808636dupA
CLNSRC
CLNACC RCV000186384.1,